Schöpf–Schulz–Passarge syndrome
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| Schöpf–Schulz–Passarge syndrome | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| ICD-10 | Q82.8 |
| OMIM | 224750 |
| Patient UK | Schöpf–Schulz–Passarge syndrome |
Schöpf–Schulz–Passarge syndrome (also known as "Eyelid cysts, palmoplantar keratoderma, hypodontia, and hypotrichosis") is an autosomal recessive condition with diffuse symmetric palmoplantar keratoderma, with the palmoplantar keratoderma and fragility of the nails beginning around age 12.[1]:513[2]
It was characterized in 1971.[3]
It has been associated with WNT10A.[4]
See also
- Palmoplantar keratoderma
- List of cutaneous conditions
- List of dental abnormalities associated with cutaneous conditions
- List of cutaneous neoplasms associated with systemic syndromes
References
- ↑ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.
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