UV-sensitive syndrome

Orpha code: 178338OMIM code: 614640

Definicja

A rare photodermatosis characterized by cutaneous photosensitivity and slight dyspigmentation, without an increased risk of developing skin tumors. Telangiectasia may also be observed, but no other clinical abnormalities. Patients present in infancy or childhood, mode of inheritance is autosomal recessive.

Disease data
Klasyfikacja

Disease

Kod ORPHA
178338
Kod OMIM
614640
Kod ICD10
L56.8
Kod ICD11
-

No additional description.

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