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]
| Schöpf–Schulz–Passarge syndrome | |
|---|---|
| Other names | Eyelid cysts, Palmoplantar keratoderma, Hypodontia, and Hypotrichosis |
| Specialty | Medical genetics  |
It was characterized in 1971.[4]