Knowledge (XXG)

Corneodermatoosseous syndrome

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Stevens, Howard P.; David P. Kelsell, and Irene M. Leigh (2003). "Chapter 52: The Inherited Keratodermas of Palms and Soles". In Freedberg; et al. (eds.).
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condition with onset in infancy, characterized by corneal dystrophy, photophobia,
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Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
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Template:Congenital malformations and deformations of skin appendages
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Focal palmoplantar keratoderma with oral mucosal hyperkeratosis
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This condition is inherited in an autosomal dominant manner
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Congenital hypertrophy of the lateral fold of the hallux
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Template:DNA replication and repair-deficiency disorder
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McGraw-Hill. p. 513. 46: 29: 1252:Congenital cartilaginous rest of the neck 847:Focal palmoplantar and gingival keratosis 135:"Orphanet: Corneodermatoosseous syndrome" 1317:Rapidly involuting congenital hemangioma 907:Keratosis punctata of the palmar creases 902:Keratosis punctata palmaris et plantaris 773:Clouston's hidrotic ectodermal dysplasia 125: 151: 378:Congenital ichthyosiform erythroderma 7: 1364: 1362: 1039:Keratosis pilaris atrophicans faciei 624:Dermatopathia pigmentosa reticularis 133:RESERVED, INSERM US14-- ALL RIGHTS. 1375:. You can help Knowledge (XXG) by 1332:Superficial lymphatic malformation 1277:Congenital smooth muscle hamartoma 746:Palmoplantar keratoderma of Sybert 315:malformations and deformations of 25: 804:Scleroatrophic syndrome of Huriez 634:Hypohidrotic ectodermal dysplasia 917:Porokeratosis plantaris discreta 874:Striate palmoplantar keratoderma 82:diffuse palmoplantar keratoderma 1342:Verrucous vascular malformation 1272:Congenital preauricular fistula 1242:Accessory nail of the fifth toe 1119:Template:Pigmentation disorders 912:Schöpf–Schulz–Passarge syndrome 892:Acrokeratoelastoidosis of Costa 597:Laryngoonychocutaneous syndrome 470:Ichthyosis linearis circumflexa 455:Ichthyosis prematurity syndrome 1427:Syndromes affecting the cornea 956:Erythrokeratodermia variabilis 867:Pachyonychia congenita type II 1: 1282:Cystic lymphatic malformation 1235:Cavernous venous malformation 862:Pachyonychia congenita type I 785:Corneodermatoosseous syndrome 445:Ichthyosis bullosa of Siemens 1432:Syndromes with short stature 690:Popliteal pterygium syndrome 382:Epidermolytic hyperkeratosis 114:List of cutaneous conditions 74:Corneodermatosseous syndrome 33:Corneodermatoosseous syndrom 1322:Rosenthal–Kloepfer syndrome 1307:Omphalomesenteric duct cyst 1024:Keratolytic winter erythema 684:Gerodermia osteodysplastica 1458: 1361: 897:Focal acral hyperkeratosis 644:Ellis–van Creveld syndrome 1422:Palmoplantar keratodermas 821:Papillon–Lefèvre syndrome 392:Harlequin-type ichthyosis 54: 45: 695:Pseudoxanthoma elasticum 411:Sjögren–Larsson syndrome 94:Palmoplantar keratoderma 1437:Syndromes with dysmelia 1220:Aplasia cutis congenita 639:Focal dermal hypoplasia 602:Skin fragility syndrome 450:Ichthyosis follicularis 1337:Thyroglossal duct cyst 1302:Nasolacrimal duct cyst 1225:Amniotic band syndrome 1019:Dyskeratosis congenita 1007:Dyskeratosis congenita 857:Pachyonychia congenita 768:Bart–Pumphrey syndrome 700:Van der Woude syndrome 675:Ehlers–Danlos syndrome 1202:Nevus flammeus nuchae 1113:Template:Phakomatoses 1085:Hereditary lymphedema 649:Rapp–Hodgkin syndrome 338:Congenital ichthyosis 1442:Genodermatoses stubs 1192:Capillary hemangioma 1094:Urticaria pigmentosa 852:Howel–Evans syndrome 612:Ectodermal dysplasia 553:Generalized atrophic 879:Tyrosinemia type II 429:X-linked ichthyosis 387:Lamellar ichthyosis 360:Ichthyosis vulgaris 343:erythrokeratodermia 1262:Congenital lip pit 826:Haim–Munk syndrome 778:Vohwinkel syndrome 653:Hay–Wells syndrome 629:Hay–Wells syndrome 475:Ichthyosis hystrix 401:Netherton syndrome 256:External resources 78:autosomal dominant 1384: 1383: 1359: 1358: 1355: 1354: 1287:Median raphe cyst 1247:Bronchogenic cyst 1169:PHACE association 1133: 1132: 1052: 1051: 1044:Keratosis pilaris 988:Keratosis pilaris 942:Carvajal syndrome 922:Spiny keratoderma 587:Costello syndrome 483: 482: 279: 278: 71: 70: 27:Medical condition 16:(Redirected from 1449: 1405: 1398: 1391: 1363: 1174:Sinus pericranii 1144: 1000:Darier's disease 809:Olmsted syndrome 720: 620:Naegeli syndrome 592:Kindler syndrome 348: 334: 306: 299: 292: 283: 201: 189: 188: 170: 164: 163: 157: 149: 147: 145: 130: 66:Medical genetics 50: 30: 21: 1457: 1456: 1452: 1451: 1450: 1448: 1447: 1446: 1412: 1411: 1410: 1409: 1360: 1351: 1213:Other/ungrouped 1208: 1197:Port-wine stain 1178: 1139: 1129: 1048: 971: 713: 704: 657: 606: 491: 479: 433: 415: 364: 341: 323: 310: 280: 275: 274: 251: 250: 212: 198: 193: 192: 185: 172: 171: 167: 150: 143: 141: 132: 131: 127: 122: 90: 28: 23: 22: 15: 12: 11: 5: 1455: 1453: 1445: 1444: 1439: 1434: 1429: 1424: 1414: 1413: 1408: 1407: 1400: 1393: 1385: 1382: 1381: 1369:Genodermatoses 1357: 1356: 1353: 1352: 1350: 1349: 1344: 1339: 1334: 1329: 1324: 1319: 1314: 1312:Poland anomaly 1309: 1304: 1299: 1297:Mongolian spot 1294: 1289: 1284: 1279: 1274: 1269: 1264: 1259: 1254: 1249: 1244: 1238: 1237: 1232: 1230:Branchial cyst 1227: 1222: 1216: 1214: 1210: 1209: 1207: 1206: 1205: 1204: 1194: 1188: 1186: 1180: 1179: 1177: 1176: 1171: 1166: 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Retrieved 138: 128: 73: 72: 41:CDO syndrome 18:CDO syndrome 1327:Skin dimple 936:desmoplakin 928:ungrouped: 815:Cathepsin C 791:plakoglobin 492:and related 104:Skin lesion 99:Keratoderma 38:Other names 1416:Categories 757:syndromic 680:Cutis laxa 667:Connective 317:integument 313:Congenital 120:References 1347:Birthmark 1140:anomalies 1107:see also 585:related: 438:Ungrouped 61:Specialty 1065:cadherin 950:connexin 888:punctate 762:connexin 265:Orphanet 154:cite web 144:19 April 88:See also 1147:Midline 732:diffuse 663:Elastic 246:C536444 225:: H18.5 994:ATP2A2 558:JEB-PA 529:EBS-MP 524:EBS-MD 519:EBS-OG 514:EBS-DM 509:EBS-WC 235:122440 181:  76:is an 1367:This 1184:Nevus 1057:Other 976:Other 838:focal 548:Mitis 543:JEB-H 504:EBS-K 1373:stub 577:RDEB 572:DDEB 270:3194 241:MeSH 230:OMIM 179:ISBN 160:link 146:2019 965:KID 961:HID 724:PPK 567:DEB 538:JEB 499:EBS 218:ICD 1418:: 1122:, 1116:, 1111:, 890:: 840:: 734:: 489:EB 421:XR 380:: 370:AR 352:AD 319:/ 268:: 244:: 233:: 222:10 156:}} 152:{{ 137:. 1404:e 1397:t 1390:v 1379:. 1092:/ 963:/ 712:/ 686:) 682:( 665:/ 651:/ 622:/ 340:/ 305:e 298:t 291:v 220:- 210:D 187:. 162:) 148:. 20:)

Index

CDO syndrome

Specialty
Medical genetics
autosomal dominant
diffuse palmoplantar keratoderma
Palmoplantar keratoderma
Keratoderma
Skin lesion
Terminal osseous dysplasia with pigmentary defects
List of cutaneous conditions
"Orphanet: Corneodermatoosseous syndrome"
cite web
link
ISBN
0-07-138067-1
D
ICD
10
OMIM
122440
MeSH
C536444
Orphanet
3194
v
t
e
Congenital
integument

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