208:(also known as "Autosomal-dominant hereditary punctate keratoderma associated with malignancy", "Buschke–Fischer–Brauer disease", "Davis Colley disease", "Keratoderma disseminatum palmaris et plantaris", "Keratosis papulosa", "Keratoderma punctatum", "Keratodermia punctata", "Keratoma hereditarium dissipatum palmare et plantare", "Palmar and plantar seed dermatoses", "Palmar keratoses", "Papulotranslucent acrokeratoderma", "Punctate keratoderma", "Punctate keratoses of the palms and soles", and "Maculosa disseminata") is a skin condition, an autosomal dominant palmoplantar keratoderma with
75:
130:
149:(also known as "Palmoplantar keratoderma cum degeneratione granulosa Vörner", "Vörner's epidermolytic palmoplantar keratoderma", and "Vörner keratoderma") is one of the most common patterns of palmoplantar keratoderma, an autosomal dominant condition that presents within the first few months of life, characterized by a well-demarcated, symmetric thickening of palms and soles, often with a "dirty" snakeskin appearance due to underlying epidermolysis.
155:(also known as "Diffuse orthohyperkeratotic keratoderma", "Hereditary palmoplantar keratoderma", "Keratosis extremitatum progrediens", "Keratosis palmoplantaris diffusa circumscripta", "Tylosis", "Unna–Thost disease", and "Unna–Thost keratoderma") is inherited as an autosomal dominant condition and is present from infancy, characterized by a well-demarcated, symmetric, often "waxy"
51:
291:(also known as "Acral keratoderma", "BrĂĽnauer-Fuhs-Siemens type of palmoplantar keratoderma", "Focal non-epidermolytic palmoplantar keratoderma", "Keratosis palmoplantaris varians", "Palmoplantar keratoderma areata", "Palmoplantar keratoderma striata", "Wachter keratoderma", and "Wachters palmoplantar keratoderma") is a cutaneous condition, an autosomal dominant
265:(also known as "Greither palmoplantar keratoderma", "Greither syndrome", "Keratosis extremitatum hereditaria progrediens", "Keratosis palmoplantaris transgrediens et progrediens" "Sybert keratoderma", and "Transgrediens and progrediens palmoplantar keratoderma") is an extremely rare autosomal dominant
137:
Diffuse palmoplantar keratoderma is a type of palmoplantar keratoderma that is characterized by an even, thick, symmetric hyperkeratosis over the whole of the palm and sole, usually evident at birth or in the first few months of life. Restated, diffuse palmoplantar keratoderma is an
176:(also known as "Focal epidermolytic palmoplantar keratoderma", "Hereditary painful callosities", "Hereditary painful callosity syndrome", "Keratosis follicularis", "Keratosis palmoplantaris nummularis", and "Nummular epidermolytic palmoplantar keratoderma") is an autosomal dominant
168:
Focal palmoplantar keratoderma, a type of palmoplantar keratoderma in which large, compact masses of keratin develop at sites of recurrent friction, principally on the feet, although also on the palms and other sites, a pattern of calluses that may be discoid (nummular) or linear.
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352:(also known as "Huriez syndrome", "Palmoplantar keratoderma with scleroatrophy", "Palmoplantar keratoderma with sclerodactyly", "Scleroatrophic and keratotic dermatosis of the limbs", and "Sclerotylosis") is an autosomal dominant
333:(also known as "Striate palmoplantar keratoderma with woolly hair and cardiomyopathy" and "Striate palmoplantar keratoderma with woolly hair and left ventricular dilated cardiomyopathy",) is a cutaneous condition inherited in an
345:
forms, but only the recessive forms have a clear association with dilated cardiomyopathy. The skin disease presents as a striate palmoplantar keratoderma with some nonvolar involvement, particularly at sites of pressure or
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Garçon-Michel N, Roguedas-Contios AM, Rault G, Le Bihan J, Ramel S, Revert K, Dirou A, Misery L (July 2010). "Frequency of aquagenic palmoplantar keratoderma in cystic fibrosis: a new sign of cystic fibrosis?".
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with onset in early infancy characterized by a honeycombed keratoderma involving the palmoplantar surfaces. Mild to moderate sensorineural hearing loss is often associated. It has been associated with
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380:(also known as "Mutilating palmoplantar keratoderma with periorificial keratotic plaques", "Mutilating palmoplantar keratoderma with periorificial plaques" and "Polykeratosis of Touraine") is a
366:(also known as "Keratoderma hereditaria mutilans", "Keratoma hereditaria mutilans", "Mutilating keratoderma of Vohwinkel", "Mutilating palmoplantar keratoderma") is a diffuse autosomal dominant
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of late onset that develops in patients aged 12 to 50, characterized by multiple tiny keratotic plugs, resembling the spines on a music box, involving the entire palmoplantar surfaces.
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212:, characterized clinically by multiple, tiny, punctate keratoses over the entire palmoplantar surfaces, beginning over the lateral edge of the digits. It has been linked to 15q22-q24.
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of the palms and soles, with flexion deformity of the digits, that begins in infancy. Treatment with retinoids has been described. It has been associated with mutations in TRPV3.
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Martinez-Mir A, Zlotogorski A, Londono D, Gordon D, Grunn A, Uribe E, Horev L, Ruiz IM, Davalos NO, Alayan O, Liu J, Gilliam TC, Salas-Alanis JC, Christiano AM (December 2003).
269:(a skin condition involving horn-like growths) with symmetric severe involvement of the whole palmoplantar surface in a glove-and-stocking distribution. It was characterized by
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Gurel G, Cilingir O, Kutluay O, Arslan S, Sahin S, Colgecen E (2019) Patient with Mal de Meleda in whom a novel gene mutation was identified. Eurasian J Med 51(2):206–208
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on the palms after water exposure. The condition causes irritation of the palms when touching certain materials after being wet, e.g., paper, cloth. An association with
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Lin Z, Chen Q, Lee M, Cao X, Zhang J, Ma D, Chen L, Hu X, Wang H, Wang X, Zhang P, Liu X, Guan L, Tang Y, Yang H, Tu P, Bu D, Zhu X, Wang K, Li R, Yang Y (March 2012).
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Erkek E, Koçak M, Bozdoğan O, Atasoy P, Birol A (2004). "Focal acral hyperkeratosis: a rare cutaneous disorder within the spectrum of Costa acrokeratoelastoidosis".
219:(also known as "Porokeratosis punctata palmaris et plantaris", "Punctate keratoderma", and "Punctate porokeratosis of the palms and soles") is an autosomal dominant
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Dessureault J, Poulin Y, Bourcier M, Gagne E (2003). "Olmsted syndrome-palmoplantar and periorificial keratodermas: association with malignant melanoma".
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present at birth with a diffuse symmetric keratoderma of the palms and soles. An association with 4q23 has been described. It was characterized in 1968.
1098:"A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families"
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341:. Striate palmoplantar keratoderma, woolly hair, and left ventricular dilated cardiomyopathy has been described in both autosomal dominant and
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Gach JE, Munro CS, Lane EB, Wilson NJ, Moss C (November 2005). "Two families with
Greither's syndrome caused by a keratin 1 mutation".
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Sybert VP, Dale BA, Holbrook KA (January 1988). "Palmar-plantar keratoderma. A clinical, ultrastructural, and biochemical study".
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disorder in which hyperkeratosis is confined to the palms and soles. The two major types can have a similar clinical appearance:
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1022:"A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23"
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Maestrini E, Korge BP, Ocaña-Sierra J, Calzolari E, Cambiaghi S, Scudder PM, Hovnanian A, Monaco AP, Munro CS (July 1999).
251:(also known as "Charcot–Marie–Tooth disease with palmoplantar keratoderma and nail dystrophy") is an autosomal dominant or
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230:(also known as "Acrokeratoelastoidosis lichenoides", and "Degenerative collagenous plaques of the hand") is a late-onset
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Ryan P, Baird G, Benfanti P (March 2007). "Hereditary painful callosities: case report and review of the literature".
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developing along the border of the hands, feet, and wrists. It is considered similar to Costa acrokeratoelastoidosis.
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Clinically, three distinct patterns of palmoplantar keratoderma may be identified: diffuse, focal, and punctate.
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is a form of palmoplantar keratoderma in which many tiny "raindrop" keratoses involve the palmoplantar surface,
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which may involve the whole of the palmoplantar surface, or may be more restricted in their distribution.
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has been suggested. The association with cystic fibrosis suggests an increased salt content in the skin.
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1363:"Permanent treatment of aquagenic syringeal acrokeratoderma with endoscopic thoracic sympathectomy"
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has been described. This is associated with mutations in the
Secreted Ly-6/uPAR-related protein 1 (
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768:"Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24"
234:, inherited as an autosomal dominant condition, characterized by oval or polygonal crateriform
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principally involving the soles with onset in infancy or the first few years of life.
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Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
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Der
Hautarzt; Zeitschrift fĂĽr Dermatologie, Venerologie, und Verwandte Gebiete
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1270:"Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome"
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Patel S, Zirwas M, English JC (2007). "Acquired palmoplantar keratoderma".
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Template:Congenital malformations and deformations of skin appendages
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Nonepidermolytic palmoplantar keratoderma has been associated with
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Huriez C, Deminatti M, Agache P, Mennecier M (February 1968). "".
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Lee YA, Stevens HP, Delaporte E, Wahn U, Reis A (January 2000).
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Epidermolytic palmoplantar keratoderma has been associated with
406:, is a skin condition characterized by the development of white
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309:
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2883:
Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
2326:
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Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
4012:
Hydrops-ectopic calcification-moth-eaten skeletal dysplasia
255:
condition that begins in early childhood with thick focal
4286:
Microcephalic osteodysplastic primordial dwarfism type II
3298:
Congenital hypertrophy of the lateral fold of the hallux
1367:
Indian
Journal of Dermatology, Venereology and Leprology
3166:
Template:DNA replication and repair-deficiency disorder
1137:
Vohwinkel KH (1929). "Keratoma hereditarium mutilans".
277:
in 1988. An autosomal recessive form which is known as
4248:
Epidermolysis bullosa simplex with muscular dystrophy
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Cutaneous keratosis, ulcer, atrophy, and necrobiosis
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transient reactive papulotranslucent acrokeratoderma
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Palisaded neutrophilic and granulomatous dermatitis
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3648:Terminal osseous dysplasia with pigmentary defects
2072:Lupus erythematosus–lichen planus overlap syndrome
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259:over the soles and, to a lesser extent, the palms.
2782:Diffuse nonepidermolytic palmoplantar keratoderma
180:that represents a clinical overlap syndrome with
153:Diffuse nonepidermolytic palmoplantar keratoderma
27:Abnormal thickening of skin in the palms or soles
2506:Nonbullous congenital ichthyosiform erythroderma
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2971:Palmoplantar keratoderma and spastic paraplegia
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541:(6th ed.). New York; London: McGraw-Hill.
249:Palmoplantar keratoderma and spastic paraplegia
3781:Meesmann juvenile epithelial corneal dystrophy
3731:Meesmann juvenile epithelial corneal dystrophy
2777:Diffuse epidermolytic palmoplantar keratoderma
2120:Morphea–lichen sclerosus et atrophicus overlap
978:Journal of the American Academy of Dermatology
943:Journal of the American Academy of Dermatology
572:
570:
568:
566:
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147:Diffuse epidermolytic palmoplantar keratoderma
113:, and acquired forms have all been described.
3418:
3308:Congenital malformations of the dermatoglyphs
2338:
1583:
1361:Sezer E, Durmaz EÖ, Çetin E, Şahin S (2015).
539:Fitzpatrick's Dermatology in General Medicine
8:
4269:Arrhythmogenic right ventricular dysplasia 9
4237:Arrhythmogenic right ventricular dysplasia 8
3850:Reticular pigmented anomaly of the flexures
698:Rapini RP, Bolognia JL, Jorizzo JL (2007).
392:acquired aquagenic palmoplantar keratoderma
159:involving the whole of the palms and soles.
4032:
3668:
3456:
3447:
3425:
3411:
3403:
3333:Melanotic neuroectodermal tumor of infancy
3184:
3070:Keratosis follicularis spinulosa decalvans
2760:
2501:Ichthyosis–sclerosing cholangitis syndrome
2388:
2374:
2345:
2331:
2323:
2027:
1841:
1590:
1576:
1568:
1434:
73:
49:
32:
3293:Congenital cartilaginous rest of the neck
2888:Focal palmoplantar and gingival keratosis
1684:Seborrheic keratosis with squamous atypia
1378:
1293:
1226:Journal of Cutaneous Medicine and Surgery
1199:
1189:
1113:
1045:
858:Leonard AL, Freedberg IM (October 2003).
791:
184:but without the classic nail involvement.
3845:Naegeli–Franceschetti–Jadassohn syndrome
3358:Rapidly involuting congenital hemangioma
2948:Keratosis punctata of the palmar creases
2943:Keratosis punctata palmaris et plantaris
2814:Clouston's hidrotic ectodermal dysplasia
1925:Interstitial granulomatous drug reaction
1896:Annular elastolytic giant-cell granuloma
1718:Confluent and reticulated papillomatosis
1701:Keratosis punctata of the palmar creases
604:American Journal of Clinical Dermatology
206:Keratosis punctata palmaris et plantaris
1770:Multiple minute digitate hyperkeratosis
1755:Hyperkeratosis of the nipple and areola
468:
1627:Acrokeratosis paraneoplastica of Bazex
91:characterized by abnormal thickening (
4253:Epidermolysis bullosa simplex of Ogna
3522:DFN A3, 4, 11, 17, 22; B2, 30, 37, 48
2419:Congenital ichthyosiform erythroderma
2217:Atrophia maculosa varioliformis cutis
1921:Interstitial granulomatous dermatitis
537:Freedberg IM, Fitzpatrick TB (2003).
58:Patient with severe plantar keratosis
7:
3870:Desmin-related myofibrillar myopathy
3507:Hypertrophic cardiomyopathy 1, 8, 10
3080:Keratosis pilaris atrophicans faciei
2665:Dermatopathia pigmentosa reticularis
1745:Hyperkeratosis lenticularis perstans
1139:Archiv fĂĽr Dermatologie und Syphilis
860:"Palmoplantar keratoderma of Sybert"
577:James W, Berger T, Elston D (2005).
3962:Emery–Dreifuss muscular dystrophy 2
2197:Acrodermatitis chronica atrophicans
1417:Online Mendelian Inheritance in Man
1402:Online Mendelian Inheritance in Man
1172:Kumar P, Sharma PK, Kar HK (2008).
400:aquagenic syringeal acrokeratoderma
4227:Striate palmoplantar keratoderma 2
3922:Charcot–Marie–Tooth disease 1F, 2E
3700:Striate palmoplantar keratoderma 3
3373:Superficial lymphatic malformation
3318:Congenital smooth muscle hamartoma
2787:Palmoplantar keratoderma of Sybert
2356:malformations and deformations of
2299:Poikiloderma vasculare atrophicans
2192:Atrophoderma of Pasini and Pierini
2130:Atrophoderma of Pasini and Pierini
1320:The British Journal of Dermatology
1274:American Journal of Human Genetics
1026:American Journal of Human Genetics
263:Palmoplantar keratoderma of Sybert
25:
4078:Asphyxiating thoracic dysplasia 3
3967:Limb-girdle muscular dystrophy 1B
2845:Scleroatrophic syndrome of Huriez
2675:Hypohidrotic ectodermal dysplasia
2240:Reactive perforating collagenosis
1874:Granuloma annulare in HIV disease
702:. St. Louis: Mosby. p. 740.
350:Scleroatrophic syndrome of Huriez
273:in 1952. It was characterized by
194:Punctate palmoplantar keratoderma
4073:Short rib-polydactyly syndrome 3
4050:Hereditary spastic paraplegia 10
3545:Hypertrophic cardiomyopathy 7, 2
2958:Porokeratosis plantaris discreta
2915:Striate palmoplantar keratoderma
1689:Reticulated seborrheic keratosis
1332:10.1111/j.1365-2133.2010.09764.x
829:10.1111/j.0736-8046.2004.21208.x
616:10.2165/00128071-200708010-00001
404:aquagenic wrinkling of the palms
337:fashion, and due to a defect in
289:Striate palmoplantar keratoderma
133:Diffuse palmoplantar keratoderma
3972:Charcot–Marie–Tooth disease 2B1
3383:Verrucous vascular malformation
3313:Congenital preauricular fistula
3283:Accessory nail of the fifth toe
3160:Template:Pigmentation disorders
2953:Schöpf–Schulz–Passarge syndrome
2933:Acrokeratoelastoidosis of Costa
2638:Laryngoonychocutaneous syndrome
2511:Ichthyosis linearis circumflexa
2496:Ichthyosis prematurity syndrome
2255:Acquired perforating dermatosis
2245:Elastosis perforans serpiginosa
2185:Jadassohn–Pellizzari anetoderma
374:. It was characterized in 1929.
4181:Familial adenomatous polyposis
4135:Hereditary elliptocytosis 2, 3
4045:Charcot–Marie–Tooth disease 2A
3957:Familial partial lipodystrophy
3469:Hypertrophic cardiomyopathy 11
2997:Erythrokeratodermia variabilis
2908:Pachyonychia congenita type II
1679:Irritated seborrheic keratosis
725:Foot & Ankle International
1:
4130:Hereditary spherocytosis 2, 3
4099:Cavernous venous malformation
3927:Amyotrophic lateral sclerosis
3897:Amyotrophic lateral sclerosis
3801:Epidermolysis bullosa simplex
3751:Epidermolysis bullosa simplex
3721:Ichthyosis bullosa of Siemens
3591:Hypertrophic cardiomyopathy 9
3568:Hypertrophic cardiomyopathy 3
3323:Cystic lymphatic malformation
3276:Cavernous venous malformation
2903:Pachyonychia congenita type I
2826:Corneodermatoosseous syndrome
2486:Ichthyosis bullosa of Siemens
2212:Linear atrophoderma of Moulin
1884:Patch-type granuloma annulare
1760:Inverted follicular keratosis
1178:Indian Journal of Dermatology
990:10.1016/S0190-9622(88)70012-2
182:pachyonychia congenita type I
87:are a heterogeneous group of
3771:Epidermolytic hyperkeratosis
3705:Epidermolytic hyperkeratosis
2731:Popliteal pterygium syndrome
2423:Epidermolytic hyperkeratosis
2180:Schweninger–Buzzi anetoderma
1879:Localized granuloma annulare
457:List of cutaneous conditions
3992:Buschke–Ollendorff syndrome
3363:Rosenthal–Kloepfer syndrome
3348:Omphalomesenteric duct cyst
3065:Keratolytic winter erythema
2725:Gerodermia osteodysplastica
1906:Necrobiotic xanthogranuloma
1805:Waxy keratosis of childhood
1674:Common seborrheic keratosis
1669:Clonal seborrheic keratosis
1651:Keratoderma blennorrhagicum
914:Greither A (May 1952). "".
772:Journal of Medical Genetics
581:(10th ed.). Saunders.
4341:
4151:Hereditary spherocytosis 1
4068:Primary ciliary dyskinesia
3474:Dilated cardiomyopathy 1AA
2938:Focal acral hyperkeratosis
2685:Ellis–van Creveld syndrome
1622:Paraneoplastic keratoderma
1286:10.1016/j.ajhg.2012.02.006
955:10.1016/j.jaad.2005.01.139
864:Dermatology Online Journal
228:Focal acral hyperkeratosis
4320:Palmoplantar keratodermas
4295:
3982:Barraquer–Simons syndrome
3875:Dilated cardiomyopathy 1I
3621:Weill–Marchesani syndrome
2862:Papillon–Lefèvre syndrome
2433:Harlequin-type ichthyosis
1694:Dermatosis papulosa nigra
1617:Keratoderma climactericum
1239:10.1007/s10227-002-0107-4
700:Dermatology: 2-Volume Set
85:Palmoplantar keratodermas
57:
48:
4125:Spinocerebellar ataxia 5
3949:Mandibuloacral dysplasia
3517:Freeman–Sheldon syndrome
2736:Pseudoxanthoma elasticum
2452:Sjögren–Larsson syndrome
2250:Perforating folliculitis
2202:Semicircular lipoatrophy
1639:Drug-induced keratoderma
1380:10.4103/0378-6323.168331
1102:Human Molecular Genetics
99:of the palms and soles.
36:Palmoplantar keratoderma
4264:Skin fragility syndrome
4206:Giant axonal neuropathy
3811:Steatocystoma multiplex
3261:Aplasia cutis congenita
2680:Focal dermal hypoplasia
2643:Skin fragility syndrome
2491:Ichthyosis follicularis
2207:Follicular atrophoderma
1995:eosinophilic dermatosis
1191:10.4103/0019-5154.41657
1071:La Semaine des Hopitaux
3550:Nemaline myopathy 4, 5
3378:Thyroglossal duct cyst
3343:Nasolacrimal duct cyst
3266:Amniotic band syndrome
3060:Dyskeratosis congenita
3048:Dyskeratosis congenita
2898:Pachyonychia congenita
2809:Bart–Pumphrey syndrome
2741:Van der Woude syndrome
2716:Ehlers–Danlos syndrome
1935:Foreign body granuloma
1846:Necrobiotic/palisading
1740:Chronic scar keratosis
949:(5 Suppl 1): S225-30.
134:
4300:Cytoskeletal proteins
3243:Nevus flammeus nuchae
3154:Template:Phakomatoses
3126:Hereditary lymphedema
2690:Rapp–Hodgkin syndrome
2379:Congenital ichthyosis
2110:Localized scleroderma
1891:Necrobiosis lipoidica
1823:Cutis verticis gyrata
1750:Hydrocarbon keratosis
1634:Aquagenic keratoderma
817:Pediatric Dermatology
784:10.1136/jmg.40.12.872
737:10.3113/FAI.2007.0377
388:Aquagenic keratoderma
132:
18:Aquagenic keratoderma
3233:Capillary hemangioma
3135:Urticaria pigmentosa
2893:Howel–Evans syndrome
2653:Ectodermal dysplasia
2594:Generalized atrophic
2273:Pyoderma gangrenosum
2135:Pansclerotic morphea
1916:Rheumatoid nodulosis
1901:Granuloma multiforme
1780:Reactional keratosis
1730:Ichthyosis acquisita
1713:Acanthosis nigricans
1664:Seborrheic keratosis
1605:Epidermal thickening
1115:10.1093/hmg/8.7.1237
44:Vohwinkel's syndrome
4007:Pelger–Huet anomaly
3917:Parkinson's disease
3638:Boomerang dysplasia
3573:Nemaline myopathy 1
3527:May–Hegglin anomaly
3484:Nemaline myopathy 3
2920:Tyrosinemia type II
2470:X-linked ichthyosis
2428:Lamellar ichthyosis
2401:Ichthyosis vulgaris
2384:erythrokeratodermia
2125:Generalized morphea
1963:Zirconium granuloma
1943:Beryllium granuloma
1811:other hypertrophy:
1765:Lichenoid keratosis
1735:Arsenical keratosis
343:autosomal recessive
335:autosomal recessive
210:variable penetrance
103:Autosomal recessive
4176:Gardner's syndrome
4145:Long QT syndrome 4
3821:Familial cirrhosis
3791:White sponge nevus
3761:Familial cirrhosis
3741:White sponge nevus
3303:Congenital lip pit
2867:Haim–Munk syndrome
2819:Vohwinkel syndrome
2694:Hay–Wells syndrome
2670:Hay–Wells syndrome
2516:Ichthyosis hystrix
2442:Netherton syndrome
2145:Linear scleroderma
1958:Silicone granuloma
1854:Granuloma annulare
1542:External resources
1174:"Olmsted syndrome"
1151:10.1007/bf01826619
876:10.5070/D31QG46424
364:Vohwinkel syndrome
140:autosomal dominant
135:
4307:
4306:
4232:Carvajal syndrome
4107:
4106:
4022:
4021:
3886:Alexander disease
3658:
3657:
3599:
3598:
3512:Usher syndrome 1B
3502:Elejalde syndrome
3400:
3399:
3396:
3395:
3328:Median raphe cyst
3288:Bronchogenic cyst
3210:PHACE association
3174:
3173:
3093:
3092:
3085:Keratosis pilaris
3029:Keratosis pilaris
2983:Carvajal syndrome
2963:Spiny keratoderma
2628:Costello syndrome
2524:
2523:
2320:
2319:
2316:
2315:
2115:Localized morphea
2087:Rowell's syndrome
2011:
2010:
2001:Granuloma faciale
1948:Mercury granuloma
1818:Hypertrophic scar
1800:Warty dyskeratoma
1790:Thermal keratosis
1565:
1564:
984:(1 Pt 1): 75–86.
709:978-1-4160-2999-1
588:978-0-7216-2921-6
548:978-0-07-138076-8
331:Carvajal syndrome
253:x-linked dominant
217:Spiny keratoderma
82:
81:
30:Medical condition
16:(Redirected from
4332:
4298:Related topics:
4033:
3669:
3457:
3448:
3427:
3420:
3413:
3404:
3215:Sinus pericranii
3185:
3041:Darier's disease
2850:Olmsted syndrome
2761:
2661:Naegeli syndrome
2633:Kindler syndrome
2389:
2375:
2347:
2340:
2333:
2324:
2289:Calcinosis cutis
2170:Lichen sclerosus
2140:Morphea profunda
2028:
1953:Silica granuloma
1842:
1785:Stucco keratosis
1592:
1585:
1578:
1569:
1435:
1423:
1414:
1408:
1399:
1393:
1392:
1382:
1358:
1352:
1351:
1314:
1308:
1307:
1297:
1265:
1259:
1258:
1220:
1214:
1213:
1203:
1193:
1169:
1163:
1162:
1134:
1128:
1127:
1117:
1093:
1087:
1086:
1066:
1060:
1059:
1049:
1017:
1011:
1008:
1002:
1001:
973:
967:
966:
938:
932:
931:
911:
905:
894:
888:
887:
855:
849:
848:
812:
806:
805:
795:
763:
757:
756:
720:
714:
713:
695:
636:
635:
599:
593:
592:
574:
553:
552:
534:
390:, also known as
378:Olmsted syndrome
78:
77:
53:
33:
21:
4340:
4339:
4335:
4334:
4333:
4331:
4330:
4329:
4310:
4309:
4308:
4303:
4291:
4211:
4155:
4103:
4082:
4054:
4018:
3997:Osteopoikilosis
3931:
3901:
3854:
3654:
3643:Larsen syndrome
3616:Marfan syndrome
3595:
3577:
3554:
3531:
3488:
3437:
3431:
3401:
3392:
3254:Other/ungrouped
3249:
3238:Port-wine stain
3219:
3180:
3170:
3089:
3012:
2754:
2745:
2698:
2647:
2532:
2520:
2474:
2456:
2405:
2382:
2364:
2351:
2321:
2312:
2277:
2259:
2221:
2160:
2151:
2100:
2091:
2033:
2032:Cutaneous lupus
2020:
2007:
1987:Other/ungrouped
1982:
1929:
1827:
1795:Viral keratosis
1599:
1596:
1566:
1561:
1560:
1537:
1536:
1446:
1432:
1427:
1426:
1415:
1411:
1400:
1396:
1360:
1359:
1355:
1316:
1315:
1311:
1267:
1266:
1262:
1222:
1221:
1217:
1171:
1170:
1166:
1136:
1135:
1131:
1095:
1094:
1090:
1068:
1067:
1063:
1019:
1018:
1014:
1009:
1005:
975:
974:
970:
940:
939:
935:
913:
912:
908:
895:
891:
857:
856:
852:
814:
813:
809:
765:
764:
760:
722:
721:
717:
710:
697:
696:
639:
601:
600:
596:
589:
576:
575:
556:
549:
536:
535:
470:
465:
448:
421:
412:cystic fibrosis
275:Virginia Sybert
245:
191:
166:
127:
119:
97:stratum corneum
72:
31:
28:
23:
22:
15:
12:
11:
5:
4338:
4336:
4328:
4327:
4322:
4312:
4311:
4305:
4304:
4296:
4293:
4292:
4290:
4289:
4272:
4271:
4266:
4256:
4255:
4250:
4240:
4239:
4234:
4229:
4219:
4217:
4213:
4212:
4210:
4209:
4197:
4194:Naxos syndrome
4185:
4184:
4183:
4178:
4165:
4163:
4157:
4156:
4154:
4153:
4138:
4137:
4132:
4127:
4117:
4115:
4109:
4108:
4105:
4104:
4102:
4101:
4096:
4090:
4088:
4084:
4083:
4081:
4080:
4075:
4070:
4064:
4062:
4056:
4055:
4053:
4052:
4047:
4041:
4039:
4030:
4024:
4023:
4020:
4019:
4017:
4016:
4015:
4014:
4009:
4001:
4000:
3999:
3994:
3986:
3985:
3984:
3976:
3975:
3974:
3969:
3964:
3959:
3951:
3939:
3937:
3933:
3932:
3930:
3929:
3924:
3919:
3909:
3907:
3903:
3902:
3900:
3899:
3889:
3888:
3878:
3877:
3872:
3862:
3860:
3856:
3855:
3853:
3852:
3847:
3842:
3824:
3814:
3804:
3794:
3784:
3774:
3764:
3754:
3744:
3734:
3724:
3714:
3713:
3712:
3707:
3702:
3691:hyperkeratosis
3675:
3673:
3666:
3660:
3659:
3656:
3655:
3653:
3652:
3651:
3650:
3645:
3640:
3635:
3625:
3624:
3623:
3618:
3607:
3605:
3601:
3600:
3597:
3596:
3594:
3593:
3587:
3585:
3579:
3578:
3576:
3575:
3570:
3564:
3562:
3556:
3555:
3553:
3552:
3547:
3541:
3539:
3533:
3532:
3530:
3529:
3524:
3519:
3514:
3509:
3504:
3498:
3496:
3490:
3489:
3487:
3486:
3481:
3476:
3471:
3465:
3463:
3454:
3445:
3443:Microfilaments
3439:
3438:
3432:
3430:
3429:
3422:
3415:
3407:
3398:
3397:
3394:
3393:
3391:
3390:
3385:
3380:
3375:
3370:
3365:
3360:
3355:
3353:Poland anomaly
3350:
3345:
3340:
3338:Mongolian spot
3335:
3330:
3325:
3320:
3315:
3310:
3305:
3300:
3295:
3290:
3285:
3279:
3278:
3273:
3271:Branchial cyst
3268:
3263:
3257:
3255:
3251:
3250:
3248:
3247:
3246:
3245:
3235:
3229:
3227:
3221:
3220:
3218:
3217:
3212:
3207:
3202:
3197:
3191:
3189:
3182:
3176:
3175:
3172:
3171:
3145:
3144:
3139:
3138:
3137:
3128:
3116:
3115:
3114:
3101:
3099:
3095:
3094:
3091:
3090:
3088:
3087:
3082:
3077:
3072:
3067:
3062:
3056:
3055:
3053:Lelis syndrome
3050:
3045:
3044:
3043:
3031:
3026:
3024:Meleda disease
3020:
3018:
3014:
3013:
3011:
3010:
3009:
3008:
2999:
2987:
2986:
2985:
2973:
2966:
2965:
2960:
2955:
2950:
2945:
2940:
2935:
2925:
2924:
2923:
2922:
2917:
2912:
2911:
2910:
2905:
2895:
2890:
2885:
2876:
2874:Camisa disease
2871:
2870:
2869:
2864:
2852:
2847:
2842:
2841:
2840:
2838:Naxos syndrome
2828:
2823:
2822:
2821:
2816:
2811:
2795:
2794:
2792:Meleda disease
2789:
2784:
2779:
2769:
2767:
2758:
2751:Hyperkeratosis
2747:
2746:
2744:
2743:
2738:
2733:
2728:
2718:
2712:
2710:
2700:
2699:
2697:
2696:
2687:
2682:
2677:
2672:
2667:
2657:
2655:
2649:
2648:
2646:
2645:
2640:
2635:
2630:
2623:
2622:
2621:
2620:
2615:
2604:
2603:
2602:
2601:
2596:
2591:
2586:
2575:
2574:
2573:
2572:
2567:
2562:
2557:
2552:
2547:
2536:
2534:
2526:
2525:
2522:
2521:
2519:
2518:
2513:
2508:
2503:
2498:
2493:
2488:
2482:
2480:
2476:
2475:
2473:
2472:
2466:
2464:
2458:
2457:
2455:
2454:
2449:
2447:CHIME syndrome
2444:
2438:
2437:
2436:
2435:
2425:
2415:
2413:
2407:
2406:
2404:
2403:
2397:
2395:
2386:
2372:
2370:Genodermatosis
2366:
2365:
2352:
2350:
2349:
2342:
2335:
2327:
2318:
2317:
2314:
2313:
2311:
2310:
2301:
2296:
2291:
2285:
2283:
2279:
2278:
2276:
2275:
2269:
2267:
2261:
2260:
2258:
2257:
2252:
2247:
2242:
2237:
2231:
2229:
2223:
2222:
2220:
2219:
2214:
2209:
2204:
2199:
2194:
2189:
2188:
2187:
2182:
2172:
2166:
2164:
2153:
2152:
2150:
2149:
2148:
2147:
2142:
2137:
2132:
2127:
2122:
2117:
2106:
2104:
2093:
2092:
2090:
2089:
2084:
2079:
2074:
2069:
2062:
2061:
2051:
2050:
2045:
2038:
2036:
2025:
2013:
2012:
2009:
2008:
2006:
2005:
2004:
2003:
1990:
1988:
1984:
1983:
1981:
1980:
1975:
1970:
1965:
1960:
1955:
1950:
1945:
1939:
1937:
1931:
1930:
1928:
1927:
1918:
1913:
1908:
1903:
1898:
1893:
1888:
1887:
1886:
1881:
1876:
1871:
1866:
1861:
1850:
1848:
1839:
1829:
1828:
1826:
1825:
1820:
1815:
1808:
1807:
1802:
1797:
1792:
1787:
1782:
1777:
1775:PUVA keratosis
1772:
1767:
1762:
1757:
1752:
1747:
1742:
1737:
1732:
1727:
1722:
1721:
1720:
1709:hyperkeratosis
1704:
1703:
1698:
1697:
1696:
1691:
1686:
1681:
1676:
1671:
1656:
1655:
1654:
1653:
1641:
1636:
1631:
1630:
1629:
1619:
1609:
1607:
1601:
1600:
1597:
1595:
1594:
1587:
1580:
1572:
1563:
1562:
1559:
1558:
1546:
1545:
1543:
1539:
1538:
1535:
1534:
1523:
1512:
1501:
1487:
1468:
1447:
1442:
1441:
1439:
1438:Classification
1431:
1430:External links
1428:
1425:
1424:
1409:
1394:
1353:
1309:
1260:
1215:
1164:
1145:(2): 354–364.
1129:
1108:(7): 1237–43.
1088:
1061:
1038:10.1086/302718
1012:
1003:
968:
933:
922:(5): 198–203.
906:
889:
850:
807:
758:
715:
708:
637:
594:
587:
554:
547:
467:
466:
464:
461:
460:
459:
454:
447:
444:
420:
417:
416:
415:
385:
375:
361:
347:
328:
327:
326:
316:
306:
286:
271:Aloys Greither
260:
244:
241:
240:
239:
224:
213:
190:
187:
186:
185:
165:
162:
161:
160:
150:
126:
123:
118:
115:
89:skin disorders
80:
79:
66:
60:
59:
55:
54:
46:
45:
42:
38:
37:
29:
26:
24:
14:
13:
10:
9:
6:
4:
3:
2:
4337:
4326:
4325:Foot diseases
4323:
4321:
4318:
4317:
4315:
4302:
4301:
4294:
4287:
4283:
4282:
4277:
4274:
4273:
4270:
4267:
4265:
4261:
4258:
4257:
4254:
4251:
4249:
4245:
4242:
4241:
4238:
4235:
4233:
4230:
4228:
4224:
4221:
4220:
4218:
4214:
4207:
4203:
4202:
4198:
4195:
4191:
4190:
4186:
4182:
4179:
4177:
4174:
4173:
4172:
4171:
4167:
4166:
4164:
4162:
4158:
4152:
4149:
4148:
4147:
4146:
4142:
4136:
4133:
4131:
4128:
4126:
4122:
4119:
4118:
4116:
4114:
4110:
4100:
4097:
4095:
4092:
4091:
4089:
4085:
4079:
4076:
4074:
4071:
4069:
4066:
4065:
4063:
4061:
4057:
4051:
4048:
4046:
4043:
4042:
4040:
4038:
4034:
4031:
4029:
4025:
4013:
4010:
4008:
4005:
4004:
4002:
3998:
3995:
3993:
3990:
3989:
3987:
3983:
3980:
3979:
3977:
3973:
3970:
3968:
3965:
3963:
3960:
3958:
3955:
3952:
3950:
3947:
3946:
3944:
3941:
3940:
3938:
3934:
3928:
3925:
3923:
3920:
3918:
3914:
3913:Neurofilament
3911:
3910:
3908:
3904:
3898:
3894:
3891:
3890:
3887:
3883:
3880:
3879:
3876:
3873:
3871:
3867:
3864:
3863:
3861:
3857:
3851:
3848:
3846:
3843:
3840:
3836:
3832:
3828:
3825:
3822:
3818:
3815:
3812:
3808:
3805:
3802:
3798:
3795:
3792:
3788:
3785:
3782:
3778:
3775:
3772:
3768:
3765:
3762:
3758:
3755:
3752:
3748:
3745:
3742:
3738:
3735:
3732:
3728:
3725:
3722:
3718:
3715:
3711:
3708:
3706:
3703:
3701:
3698:
3697:
3696:
3692:
3688:
3684:
3680:
3679:Keratinopathy
3677:
3676:
3674:
3670:
3667:
3665:
3661:
3649:
3646:
3644:
3641:
3639:
3636:
3634:
3633:FG syndrome 2
3631:
3630:
3629:
3626:
3622:
3619:
3617:
3614:
3613:
3612:
3609:
3608:
3606:
3602:
3592:
3589:
3588:
3586:
3584:
3580:
3574:
3571:
3569:
3566:
3565:
3563:
3561:
3557:
3551:
3548:
3546:
3543:
3542:
3540:
3538:
3534:
3528:
3525:
3523:
3520:
3518:
3515:
3513:
3510:
3508:
3505:
3503:
3500:
3499:
3497:
3495:
3491:
3485:
3482:
3480:
3477:
3475:
3472:
3470:
3467:
3466:
3464:
3462:
3458:
3455:
3453:
3449:
3446:
3444:
3440:
3435:
3428:
3423:
3421:
3416:
3414:
3409:
3408:
3405:
3389:
3386:
3384:
3381:
3379:
3376:
3374:
3371:
3369:
3366:
3364:
3361:
3359:
3356:
3354:
3351:
3349:
3346:
3344:
3341:
3339:
3336:
3334:
3331:
3329:
3326:
3324:
3321:
3319:
3316:
3314:
3311:
3309:
3306:
3304:
3301:
3299:
3296:
3294:
3291:
3289:
3286:
3284:
3281:
3280:
3277:
3274:
3272:
3269:
3267:
3264:
3262:
3259:
3258:
3256:
3252:
3244:
3241:
3240:
3239:
3236:
3234:
3231:
3230:
3228:
3226:
3222:
3216:
3213:
3211:
3208:
3206:
3203:
3201:
3200:Encephalocele
3198:
3196:
3193:
3192:
3190:
3186:
3183:
3179:Developmental
3177:
3169:
3168:
3167:
3162:
3161:
3156:
3155:
3151:
3143:
3142:Hailey–Hailey
3140:
3136:
3132:
3129:
3127:
3124:
3123:
3122:
3121:
3120:immune system
3117:
3113:
3110:
3109:
3108:
3107:
3103:
3102:
3100:
3096:
3086:
3083:
3081:
3078:
3076:
3073:
3071:
3068:
3066:
3063:
3061:
3058:
3057:
3054:
3051:
3049:
3046:
3042:
3039:
3038:
3037:
3036:
3032:
3030:
3027:
3025:
3022:
3021:
3019:
3015:
3007:
3003:
3000:
2998:
2995:
2994:
2993:
2992:
2988:
2984:
2981:
2980:
2979:
2978:
2974:
2972:
2968:
2967:
2964:
2961:
2959:
2956:
2954:
2951:
2949:
2946:
2944:
2941:
2939:
2936:
2934:
2930:
2927:
2926:
2921:
2918:
2916:
2913:
2909:
2906:
2904:
2901:
2900:
2899:
2896:
2894:
2891:
2889:
2886:
2884:
2880:
2877:
2875:
2872:
2868:
2865:
2863:
2860:
2859:
2858:
2857:
2853:
2851:
2848:
2846:
2843:
2839:
2836:
2835:
2834:
2833:
2829:
2827:
2824:
2820:
2817:
2815:
2812:
2810:
2807:
2806:
2805:
2804:
2800:
2799:
2797:
2796:
2793:
2790:
2788:
2785:
2783:
2780:
2778:
2774:
2771:
2770:
2768:
2766:
2762:
2759:
2757:
2756:keratinopathy
2752:
2748:
2742:
2739:
2737:
2734:
2732:
2729:
2726:
2722:
2719:
2717:
2714:
2713:
2711:
2709:
2705:
2701:
2695:
2691:
2688:
2686:
2683:
2681:
2678:
2676:
2673:
2671:
2668:
2666:
2662:
2659:
2658:
2656:
2654:
2650:
2644:
2641:
2639:
2636:
2634:
2631:
2629:
2625:
2624:
2619:
2616:
2614:
2611:
2610:
2609:
2606:
2605:
2600:
2597:
2595:
2592:
2590:
2587:
2585:
2582:
2581:
2580:
2577:
2576:
2571:
2568:
2566:
2563:
2561:
2558:
2556:
2553:
2551:
2548:
2546:
2543:
2542:
2541:
2538:
2537:
2535:
2531:
2527:
2517:
2514:
2512:
2509:
2507:
2504:
2502:
2499:
2497:
2494:
2492:
2489:
2487:
2484:
2483:
2481:
2477:
2471:
2468:
2467:
2465:
2463:
2459:
2453:
2450:
2448:
2445:
2443:
2440:
2439:
2434:
2431:
2430:
2429:
2426:
2424:
2420:
2417:
2416:
2414:
2412:
2408:
2402:
2399:
2398:
2396:
2394:
2390:
2387:
2385:
2380:
2376:
2373:
2371:
2367:
2363:
2359:
2355:
2348:
2343:
2341:
2336:
2334:
2329:
2328:
2325:
2309:
2308:Pseudo-ainhum
2305:
2302:
2300:
2297:
2295:
2294:Sclerodactyly
2292:
2290:
2287:
2286:
2284:
2280:
2274:
2271:
2270:
2268:
2266:
2262:
2256:
2253:
2251:
2248:
2246:
2243:
2241:
2238:
2236:
2235:Kyrle disease
2233:
2232:
2230:
2228:
2224:
2218:
2215:
2213:
2210:
2208:
2205:
2203:
2200:
2198:
2195:
2193:
2190:
2186:
2183:
2181:
2178:
2177:
2176:
2173:
2171:
2168:
2167:
2165:
2163:
2158:
2154:
2146:
2143:
2141:
2138:
2136:
2133:
2131:
2128:
2126:
2123:
2121:
2118:
2116:
2113:
2112:
2111:
2108:
2107:
2105:
2103:
2098:
2094:
2088:
2085:
2083:
2080:
2078:
2075:
2073:
2070:
2068:
2064:
2063:
2060:
2056:
2053:
2052:
2049:
2046:
2044:
2040:
2039:
2037:
2035:
2034:erythematosus
2029:
2026:
2024:
2018:
2014:
2002:
1999:
1998:
1997:
1996:
1992:
1991:
1989:
1985:
1979:
1976:
1974:
1971:
1969:
1966:
1964:
1961:
1959:
1956:
1954:
1951:
1949:
1946:
1944:
1941:
1940:
1938:
1936:
1932:
1926:
1922:
1919:
1917:
1914:
1912:
1909:
1907:
1904:
1902:
1899:
1897:
1894:
1892:
1889:
1885:
1882:
1880:
1877:
1875:
1872:
1870:
1867:
1865:
1862:
1860:
1857:
1856:
1855:
1852:
1851:
1849:
1847:
1843:
1840:
1838:
1834:
1830:
1824:
1821:
1819:
1816:
1814:
1810:
1809:
1806:
1803:
1801:
1798:
1796:
1793:
1791:
1788:
1786:
1783:
1781:
1778:
1776:
1773:
1771:
1768:
1766:
1763:
1761:
1758:
1756:
1753:
1751:
1748:
1746:
1743:
1741:
1738:
1736:
1733:
1731:
1728:
1726:
1723:
1719:
1716:
1715:
1714:
1710:
1706:
1705:
1702:
1699:
1695:
1692:
1690:
1687:
1685:
1682:
1680:
1677:
1675:
1672:
1670:
1667:
1666:
1665:
1661:
1658:
1657:
1652:
1649:
1648:
1647:
1646:
1642:
1640:
1637:
1635:
1632:
1628:
1625:
1624:
1623:
1620:
1618:
1614:
1611:
1610:
1608:
1606:
1602:
1593:
1588:
1586:
1581:
1579:
1574:
1573:
1570:
1557:
1553:
1552:
1548:
1547:
1544:
1540:
1533:
1529:
1528:
1524:
1522:
1518:
1517:
1513:
1511:
1507:
1506:
1502:
1500:
1497:
1493:
1492:
1488:
1486:
1482:
1478:
1477:
1473:
1469:
1466:
1462:
1458:
1457:
1453:
1449:
1448:
1445:
1440:
1436:
1429:
1422:
1418:
1413:
1410:
1407:
1403:
1398:
1395:
1390:
1386:
1381:
1376:
1373:(6): 648–50.
1372:
1368:
1364:
1357:
1354:
1349:
1345:
1341:
1337:
1333:
1329:
1325:
1321:
1313:
1310:
1305:
1301:
1296:
1291:
1287:
1283:
1280:(3): 558–64.
1279:
1275:
1271:
1264:
1261:
1256:
1252:
1248:
1244:
1240:
1236:
1233:(3): 236–42.
1232:
1228:
1227:
1219:
1216:
1211:
1207:
1202:
1197:
1192:
1187:
1183:
1179:
1175:
1168:
1165:
1160:
1156:
1152:
1148:
1144:
1140:
1133:
1130:
1125:
1121:
1116:
1111:
1107:
1103:
1099:
1092:
1089:
1084:
1080:
1076:
1073:(in French).
1072:
1065:
1062:
1057:
1053:
1048:
1043:
1039:
1035:
1032:(1): 326–30.
1031:
1027:
1023:
1016:
1013:
1007:
1004:
999:
995:
991:
987:
983:
979:
972:
969:
964:
960:
956:
952:
948:
944:
937:
934:
929:
925:
921:
917:
910:
907:
904:
903:Who Named It?
900:
899:
893:
890:
885:
881:
877:
873:
869:
865:
861:
854:
851:
846:
842:
838:
834:
830:
826:
823:(2): 128–30.
822:
818:
811:
808:
803:
799:
794:
789:
785:
781:
778:(12): 872–8.
777:
773:
769:
762:
759:
754:
750:
746:
742:
738:
734:
730:
726:
719:
716:
711:
705:
701:
694:
692:
690:
688:
686:
684:
682:
680:
678:
676:
674:
672:
670:
668:
666:
664:
662:
660:
658:
656:
654:
652:
650:
648:
646:
644:
642:
638:
633:
629:
625:
621:
617:
613:
609:
605:
598:
595:
590:
584:
580:
573:
571:
569:
567:
565:
563:
561:
559:
555:
550:
544:
540:
533:
531:
529:
527:
525:
523:
521:
519:
517:
515:
513:
511:
509:
507:
505:
503:
501:
499:
497:
495:
493:
491:
489:
487:
485:
483:
481:
479:
477:
475:
473:
469:
462:
458:
455:
453:
450:
449:
445:
443:
441:
437:
432:
430:
426:
418:
413:
409:
405:
401:
397:
393:
389:
386:
383:
379:
376:
373:
369:
365:
362:
359:
358:sclerodactyly
355:
351:
348:
344:
340:
336:
332:
329:
325:
321:
317:
315:
311:
307:
305:
301:
297:
296:
294:
290:
287:
284:
280:
279:Mal de Meleda
276:
272:
268:
264:
261:
258:
254:
250:
247:
246:
242:
237:
233:
229:
225:
222:
218:
214:
211:
207:
203:
202:
201:
199:
195:
188:
183:
179:
175:
172:
171:
170:
163:
158:
154:
151:
148:
145:
144:
143:
141:
131:
124:
122:
116:
114:
112:
108:
104:
100:
98:
94:
90:
86:
76:
70:
67:
65:
61:
56:
52:
47:
43:
39:
34:
19:
4297:
4279:
4231:
4226:
4199:
4187:
4168:
4139:
4028:Microtubules
3699:
3434:Cytoskeletal
3205:Nasal glioma
3195:Dermoid cyst
3164:
3158:
3147:
3146:
3131:Mastocytosis
3118:
3112:EEM syndrome
3104:
3033:
2989:
2982:
2975:
2970:
2928:
2914:
2882:
2878:
2854:
2830:
2801:
2786:
2781:
2776:
2772:
2764:
2362:skin disease
2162:atrophoderma
2048:Panniculitis
1993:
1978:Carbon stain
1869:Subcutaneous
1643:
1633:
1549:
1525:
1514:
1503:
1489:
1470:
1450:
1412:
1397:
1370:
1366:
1356:
1326:(1): 162–6.
1323:
1319:
1312:
1277:
1273:
1263:
1230:
1224:
1218:
1181:
1177:
1167:
1142:
1138:
1132:
1105:
1101:
1091:
1077:(8): 481–8.
1074:
1070:
1064:
1029:
1025:
1015:
1006:
981:
977:
971:
946:
942:
936:
919:
915:
909:
896:
892:
867:
863:
853:
820:
816:
810:
775:
771:
761:
731:(3): 377–8.
728:
724:
718:
699:
607:
603:
597:
578:
538:
433:
422:
403:
399:
395:
391:
387:
377:
363:
349:
330:
288:
262:
248:
227:
216:
205:
198:skin lesions
193:
192:
173:
167:
152:
146:
136:
120:
101:
84:
83:
4260:plakophilin
4223:desmoplakin
4189:plakoglobin
3943:Laminopathy
3839:Monilethrix
3687:keratoderma
3560:Tropomyosin
3452:Myofilament
3368:Skin dimple
2977:desmoplakin
2969:ungrouped:
2856:Cathepsin C
2832:plakoglobin
2533:and related
2227:Perforating
2097:Scleroderma
2065:ungrouped:
1968:Soot tattoo
1864:Generalized
1859:Perforating
1833:Necrobiosis
1613:keratoderma
1184:(2): 93–5.
610:(1): 1–11.
452:Keratoderma
382:keratoderma
368:keratoderma
354:keratoderma
339:desmoplakin
293:keratoderma
267:keratoderma
257:keratoderma
232:keratoderma
221:keratoderma
178:keratoderma
157:keratoderma
93:scleroderma
69:Dermatology
41:Other names
4314:Categories
4276:centrosome
3893:Peripherin
2798:syndromic
2721:Cutis laxa
2708:Connective
2358:integument
2354:Congenital
2265:Skin ulcer
2175:Anetoderma
2041:chronic:
2021:localized
1516:DiseasesDB
463:References
440:keratin 16
429:keratin 16
4094:Tauopathy
3683:keratosis
3611:Fibrillin
3388:Birthmark
3181:anomalies
3148:see also
2626:related:
2479:Ungrouped
2082:Verrucous
2067:Chilblain
1837:granuloma
1660:keratosis
1645:psoriasis
1551:eMedicine
1532:706885006
1527:SNOMED CT
898:synd/1800
870:(4): 30.
436:keratin 1
425:keratin 9
346:abrasion.
318:Type 3:
308:Type 2:
298:Type 1:
243:Ungrouped
95:) of the
64:Specialty
4121:Spectrin
4113:Membrane
3954:Dunnigan
3537:Troponin
3106:cadherin
2991:connexin
2929:punctate
2803:connexin
2157:Atrophic
2059:Neonatal
2055:subacute
1556:derm/589
1419:(OMIM):
1404:(OMIM):
1389:26515860
1348:26018635
1340:20302572
1304:22405088
1255:23612959
1247:12704531
1210:19881998
1124:10369869
1056:10631162
963:16227096
928:14945735
884:14594603
845:19811383
837:15078352
802:14684683
753:10787216
745:17371662
624:17298101
446:See also
419:Genetics
226:Type 3:
215:Type 2:
204:Type 1:
189:Punctate
111:X-linked
107:dominant
4244:plectin
4161:Catenin
4141:Ankyrin
4037:Kinesin
3945:: LMNA
3628:Filamin
3436:defects
3188:Midline
2773:diffuse
2704:Elastic
2102:Morphea
2043:Discoid
1510:D007645
1467:, Q82.8
1295:3309189
1201:2763718
1159:1737564
1083:4298032
1047:1288338
998:2450111
793:1735333
632:7221815
408:papules
285:) gene.
236:papules
125:Diffuse
4060:Dynein
3988:LEMD3
3866:Desmin
3494:Myosin
3479:DFNA20
3035:ATP2A2
2599:JEB-PA
2570:EBS-MP
2565:EBS-MD
2560:EBS-OG
2555:EBS-DM
2550:EBS-WC
2304:Ainhum
2017:Dermis
1973:Tattoo
1813:Keloid
1725:Callus
1707:other
1499:600962
1496:144200
1485:757.39
1421:600962
1406:144200
1387:
1346:
1338:
1302:
1292:
1253:
1245:
1208:
1198:
1157:
1122:
1081:
1054:
1044:
996:
961:
926:
882:
843:
835:
800:
790:
751:
743:
706:
630:
622:
585:
545:
402:, and
320:607654
310:612908
300:148700
283:SLURP1
71:
4216:Other
4087:Other
3978:LMNB
3835:KRT86
3831:KRT83
3827:KRT81
3817:KRT18
3807:KRT17
3797:KRT14
3787:KRT13
3777:KRT12
3767:KRT10
3717:KRT2E
3604:Other
3583:Titin
3461:Actin
3225:Nevus
3098:Other
3017:Other
2879:focal
2589:Mitis
2584:JEB-H
2545:EBS-K
2282:Other
2077:Tumid
1521:32042
1481:701.1
1465:L85.2
1461:L85.1
1344:S2CID
1251:S2CID
1155:S2CID
841:S2CID
749:S2CID
628:S2CID
356:with
164:Focal
117:Types
4281:PCNT
4003:LBR
3882:GFAP
3757:KRT8
3747:KRT5
3737:KRT4
3727:KRT3
3710:IHCM
3695:KRT1
2618:RDEB
2613:DDEB
1505:MeSH
1491:OMIM
1476:9-CM
1385:PMID
1336:PMID
1300:PMID
1243:PMID
1206:PMID
1120:PMID
1079:PMID
1052:PMID
994:PMID
959:PMID
924:PMID
880:PMID
833:PMID
798:PMID
741:PMID
704:ISBN
620:PMID
583:ISBN
543:ISBN
438:and
427:and
372:GJB2
324:KRT1
304:DSG1
4201:GAN
4170:APC
3693:):
3672:1/2
3006:KID
3002:HID
2765:PPK
2608:DEB
2579:JEB
2540:EBS
2023:CTD
1472:ICD
1452:ICD
1375:doi
1328:doi
1324:163
1290:PMC
1282:doi
1235:doi
1196:PMC
1186:doi
1147:doi
1143:158
1110:doi
1042:PMC
1034:doi
986:doi
951:doi
901:at
872:doi
825:doi
788:PMC
780:doi
733:doi
612:doi
314:DSP
4316::
4278::
4262::
4246::
4225::
4143::
4123::
3915::
3895::
3884::
3868::
3689:,
3685:,
3664:IF
3163:,
3157:,
3152:,
2931::
2881::
2775::
2530:EB
2462:XR
2421::
2411:AR
2393:AD
2360:/
2057::
1711::
1662::
1615::
1554::
1530::
1519::
1508::
1494::
1483:,
1479::
1459::
1456:10
1383:.
1371:81
1369:.
1365:.
1342:.
1334:.
1322:.
1298:.
1288:.
1278:90
1276:.
1272:.
1249:.
1241:.
1229:.
1204:.
1194:.
1182:53
1180:.
1176:.
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1104:.
1100:.
1075:44
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1028:.
1024:.
992:.
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980:.
957:.
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945:.
918:.
878:.
866:.
862:.
839:.
831:.
821:21
819:.
796:.
786:.
776:40
774:.
770:.
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739:.
729:28
727:.
640:^
626:.
618:.
606:.
557:^
471:^
442:.
431:.
398:,
394:,
322::
312::
302::
109:,
105:,
4288:)
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4196:)
4192:(
3936:5
3906:4
3859:3
3841:)
3837:(
3833:/
3829:/
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3813:)
3809:(
3803:)
3799:(
3793:)
3789:(
3783:)
3779:(
3773:)
3769:(
3763:)
3759:(
3753:)
3749:(
3743:)
3739:(
3733:)
3729:(
3723:)
3719:(
3681:(
3426:e
3419:t
3412:v
3133:/
3004:/
2753:/
2727:)
2723:(
2706:/
2692:/
2663:/
2381:/
2346:e
2339:t
2332:v
2306:/
2159:/
2099:/
2019:/
1923:/
1835:/
1591:e
1584:t
1577:v
1474:-
1463:-
1454:-
1444:D
1391:.
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