Schöpf–Schulz–Passarge syndrome | |
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Other names | Eyelid cysts, Palmoplantar keratoderma, Hypodontia, and Hypotrichosis |
Specialty |
Medical genetics
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Schöpf–Schulz–Passarge syndrome is an autosomal recessive condition with punctate symmetric palmoplantar keratoderma, with the keratoderma and fragility of the nails beginning around age 12. [1]: 513 [2] In addition to palmoplantar keratoderma, other symptoms include hypodontia, hypotrichosis, nail dystrophies, and eyelid cysts ( apocrine hidrocystomas). Patients may also develop syringofibroadenoma and squamous cell carcinomas. [3]
It was characterized in 1971. [4]
It has been associated with WNT10A. [5]
Schöpf–Schulz–Passarge syndrome | |
---|---|
Other names | Eyelid cysts, Palmoplantar keratoderma, Hypodontia, and Hypotrichosis |
Specialty |
Medical genetics
![]() |
Schöpf–Schulz–Passarge syndrome is an autosomal recessive condition with punctate symmetric palmoplantar keratoderma, with the keratoderma and fragility of the nails beginning around age 12. [1]: 513 [2] In addition to palmoplantar keratoderma, other symptoms include hypodontia, hypotrichosis, nail dystrophies, and eyelid cysts ( apocrine hidrocystomas). Patients may also develop syringofibroadenoma and squamous cell carcinomas. [3]
It was characterized in 1971. [4]
It has been associated with WNT10A. [5]