Syndactyly-polydactyly-ear lobe syndrome

Orpha code: 3259OMIM code: 186350

Definicja

A rare, genetic, congenital limb malformation syndrome characterized by complete cutaneous syndactyly between toes 1-2, ulnar polydactyly (ranging from nubbins to an almost complete additional finger) and earlobe malformations. Additionally, abnormalities along the medial border of the foot are observed on X-ray imaging. There have been no further descriptions in the literature since 1976.

Disease data
Klasyfikacja

Malformation syndrome

Kod ORPHA
3259
Kod OMIM
186350
Kod ICD10
Q74.8
Kod ICD11
-

No additional description.

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