Peeling skin syndrome
From Infogalactic: the planetary knowledge core
| Peeling skin syndrome | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | Q80.8 |
| OMIM | 270300 |
| Patient UK | Peeling skin syndrome |
Peeling skin syndrome (also known as "Acral peeling skin syndrome," "Continual peeling skin syndrome," "Familial continual skin peeling," "Idiopathic deciduous skin," and "Keratolysis exfoliativa congenita"[1]) is an autosomal recessive disorder characterized by lifelong peeling of the stratum corneum, and may be associated with pruritus, short stature, and easily removed anagen hair.[2]:502
The acral form can be associated with TGM5.[3][4]
See also
References
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 609796
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
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