Schöpf–Schulz–Passarge syndrome

From WikiMD

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]

See also

References

  1. Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.

External links


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Link to this page: <a href="http://www.wikimd.org/wiki/Sch%C3%B6pf%E2%80%93Schulz%E2%80%93Passarge_syndrome">Schöpf–Schulz–Passarge syndrome</a>

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