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256:
Ludtke, A; Genschel, J; Brabant, G; Bauditz, J; et al. (October 2005). "Hepatic steatosis in
Dunnigan-type familial partial lipodystrophy".
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132:
A and C. The condition is named after
Scottish doctor Matthew Dunnigan, who pioneered early study into the disorder.
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171:
Hegele, RA (December 2000). "Familial partial lipodystrophy: A monogenic form of the insulin resistance syndrome".
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303:"Familial partial lipodystrophy: two types of an X linked dominant syndrome, lethal in the hemizygous state"
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Hegele, RA (September 2000). "Insulin resistance in human partial lipodystrophy".
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This article about an endocrine, nutritional, or metabolic disease is a
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66:
36:
Autosomal dominant is the manner of inheritance of this condition
1291:
401:
125:
122:
417:
1023:
Hydrops-ectopic calcification-moth-eaten skeletal dysplasia
1297:
Microcephalic osteodysplastic primordial dwarfism type II
1341:
1259:
Epidermolysis bullosa simplex with muscular dystrophy
366:
1226:
1170:
1122:
1097:
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1037:
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682:
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370:
21:
1397:Endocrine, nutritional and metabolic disease stubs
659:Terminal osseous dysplasia with pigmentary defects
45:, also known as FPLD Type II and abbreviated as (
792:Meesmann juvenile epithelial corneal dystrophy
742:Meesmann juvenile epithelial corneal dystrophy
206:
204:
166:
164:
162:
1361:
429:
22:Familial Partial Lipodystrophy, Dunnigan Type
8:
1280:Arrhythmogenic right ventricular dysplasia 9
1248:Arrhythmogenic right ventricular dysplasia 8
43:Dunnigan-type familial partial lipodystrophy
861:Reticular pigmented anomaly of the flexures
1368:
1354:
1043:
679:
467:
458:
436:
422:
414:
367:
27:
18:
326:
856:Naegeli–Franceschetti–Jadassohn syndrome
259:The American Journal of Gastroenterology
158:
1264:Epidermolysis bullosa simplex of Ogna
533:DFN A3, 4, 11, 17, 22; B2, 30, 37, 48
7:
1326:
1324:
881:Desmin-related myofibrillar myopathy
518:Hypertrophic cardiomyopathy 1, 8, 10
973:Emery–Dreifuss muscular dystrophy 2
301:Köbberling, J; Dunnigan, M (1986).
1392:Conditions of the subcutaneous fat
1340:. You can help Knowledge (XXG) by
1238:Striate palmoplantar keratoderma 2
933:Charcot–Marie–Tooth disease 1F, 2E
711:Striate palmoplantar keratoderma 3
14:
1089:Asphyxiating thoracic dysplasia 3
978:Limb-girdle muscular dystrophy 1B
174:Molecular Genetics and Metabolism
128:, which is the gene that encodes
1328:
1084:Short rib-polydactyly syndrome 3
1061:Hereditary spastic paraplegia 10
556:Hypertrophic cardiomyopathy 7, 2
272:10.1111/j.1572-0241.2005.00234.x
983:Charcot–Marie–Tooth disease 2B1
214:Current Atherosclerosis Reports
1387:Genetic diseases and disorders
1192:Familial adenomatous polyposis
1146:Hereditary elliptocytosis 2, 3
1056:Charcot–Marie–Tooth disease 2A
968:Familial partial lipodystrophy
480:Hypertrophic cardiomyopathy 11
142:Familial partial lipodystrophy
73:. FPLD recapitulates the main
1:
1141:Hereditary spherocytosis 2, 3
1110:Cavernous venous malformation
938:Amyotrophic lateral sclerosis
908:Amyotrophic lateral sclerosis
812:Epidermolysis bullosa simplex
762:Epidermolysis bullosa simplex
732:Ichthyosis bullosa of Siemens
602:Hypertrophic cardiomyopathy 9
579:Hypertrophic cardiomyopathy 3
782:Epidermolytic hyperkeratosis
716:Epidermolytic hyperkeratosis
1003:Buschke–Ollendorff syndrome
307:Journal of Medical Genetics
79:insulin resistance syndrome
1413:
1323:
1162:Hereditary spherocytosis 1
1079:Primary ciliary dyskinesia
485:Dilated cardiomyopathy 1AA
1306:
993:Barraquer–Simons syndrome
886:Dilated cardiomyopathy 1I
632:Weill–Marchesani syndrome
227:10.1007/s11883-000-0078-0
109:, and early endpoints of
57:characterized by loss of
35:
26:
1136:Spinocerebellar ataxia 5
960:Mandibuloacral dysplasia
528:Freeman–Sheldon syndrome
113:. It can also result in
1275:Skin fragility syndrome
1217:Giant axonal neuropathy
822:Steatocystoma multiplex
147:Priscilla Lopes-Schliep
561:Nemaline myopathy 4, 5
187:10.1006/mgme.2000.3092
1311:Cytoskeletal proteins
319:10.1136/jmg.23.2.120
117:. FPLD results from
1018:Pelger–Huet anomaly
928:Parkinson's disease
649:Boomerang dysplasia
584:Nemaline myopathy 1
538:May–Hegglin anomaly
495:Nemaline myopathy 3
91:glucose intolerance
1187:Gardner's syndrome
1156:Long QT syndrome 4
832:Familial cirrhosis
802:White sponge nevus
772:Familial cirrhosis
752:White sponge nevus
77:attributes of the
55:insulin resistance
1349:
1348:
1318:
1317:
1243:Carvajal syndrome
1118:
1117:
1033:
1032:
897:Alexander disease
669:
668:
610:
609:
523:Usher syndrome 1B
513:Elejalde syndrome
411:
410:
115:hepatic steatosis
40:
39:
16:Medical condition
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1370:
1363:
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1332:
1325:
1309:Related topics:
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368:
341:
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87:hyperinsulinemia
59:subcutaneous fat
31:
19:
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1222:
1166:
1114:
1093:
1065:
1029:
1008:Osteopoikilosis
942:
912:
865:
665:
654:Larsen syndrome
627:Marfan syndrome
606:
588:
565:
542:
499:
448:
442:
412:
407:
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379:
365:
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266:(10): 2218–24.
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111:atherosclerosis
83:central obesity
17:
12:
11:
5:
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1205:Naxos syndrome
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805:
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785:
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718:
713:
702:hyperkeratosis
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492:
487:
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476:
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465:
456:
454:Microfilaments
450:
449:
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408:
405:
404:
393:
380:
375:
374:
372:
371:Classification
364:
363:External links
361:
343:
342:
313:(2): 120–127.
293:
248:
221:(5): 397–404.
200:
157:
156:
154:
151:
150:
149:
144:
137:
134:
130:nuclear lamins
71:gluteal region
38:
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33:
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24:
23:
15:
13:
10:
9:
6:
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957:
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952:
951:
949:
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939:
936:
934:
931:
929:
925:
924:Neurofilament
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909:
905:
902:
901:
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891:
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749:
746:
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733:
729:
726:
722:
719:
717:
714:
712:
709:
708:
707:
703:
699:
695:
691:
690:Keratinopathy
688:
687:
685:
681:
678:
676:
672:
660:
657:
655:
652:
650:
647:
645:
644:FG syndrome 2
642:
641:
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637:
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628:
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619:
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297:
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249:
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236:
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220:
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196:
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184:
181:(4): 539–44.
180:
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100:
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88:
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72:
68:
64:
60:
56:
52:
49:), is a rare
48:
44:
34:
30:
25:
20:
1342:expanding it
1335:
1320:
1308:
1290:
1210:
1198:
1179:
1150:
1039:Microtubules
964:
445:Cytoskeletal
395:
383:
358:
355:
352:
349:
346:
310:
306:
296:
263:
257:
251:
218:
212:
178:
172:
107:hypertension
103:dyslipidemia
81:, including
46:
42:
41:
1271:plakophilin
1234:desmoplakin
1200:plakoglobin
954:Laminopathy
850:Monilethrix
698:keratoderma
571:Tropomyosin
463:Myofilament
63:extremities
1381:Categories
1287:centrosome
904:Peripherin
153:References
1105:Tauopathy
694:keratosis
622:Fibrillin
119:mutations
75:metabolic
61:from the
51:monogenic
1132:Spectrin
1124:Membrane
965:Dunnigan
548:Troponin
288:23356132
280:16181372
243:38167209
235:11122771
195:11136544
136:See also
97:usually
95:diabetes
53:form of
1255:plectin
1172:Catenin
1152:Ankyrin
1048:Kinesin
956:: LMNA
639:Filamin
447:defects
392:: E88.1
337:3712389
328:1049565
1071:Dynein
999:LEMD3
877:Desmin
505:Myosin
490:DFNA20
402:151660
335:
325:
286:
278:
241:
233:
193:
99:type 2
69:, and
1227:Other
1098:Other
989:LMNB
846:KRT86
842:KRT83
838:KRT81
828:KRT18
818:KRT17
808:KRT14
798:KRT13
788:KRT12
778:KRT10
728:KRT2E
615:Other
594:Titin
472:Actin
284:S2CID
239:S2CID
67:trunk
47:FPLD2
1338:stub
1292:PCNT
1014:LBR
893:GFAP
768:KRT8
758:KRT5
748:KRT4
738:KRT3
721:IHCM
706:KRT1
397:OMIM
333:PMID
276:PMID
231:PMID
191:PMID
126:gene
123:LMNA
93:and
1212:GAN
1181:APC
704:):
683:1/2
385:ICD
323:PMC
315:doi
268:doi
264:100
223:doi
183:doi
121:in
1383::
1289::
1273::
1257::
1236::
1154::
1134::
926::
906::
895::
879::
700:,
696:,
675:IF
400::
389:10
331:.
321:.
311:23
309:.
305:.
282:.
274:.
262:.
237:.
229:.
217:.
203:^
189:.
179:71
177:.
161:^
105:,
101:,
89:,
85:,
65:,
1369:e
1362:t
1355:v
1344:.
1299:)
1295:(
1219:)
1215:(
1207:)
1203:(
947:5
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870:3
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848:(
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840:/
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824:)
820:(
814:)
810:(
804:)
800:(
794:)
790:(
784:)
780:(
774:)
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764:)
760:(
754:)
750:(
744:)
740:(
734:)
730:(
692:(
437:e
430:t
423:v
387:-
377:D
339:.
317::
290:.
270::
245:.
225::
219:2
197:.
185::
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