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ORPHA:1775· ICD-10 Q82.8· Dyskeratosis congenita

Визначення(English summary)

A rare ectodermal dysplasia syndrome that often presents with the classic triad of nail dysplasia, skin pigmentary changes, and oral leukoplakia associated with a high risk of bone marrow failure (BMF) and cancer.

Поширеність
1-9 / 1 000 000
Успадкування
Autosomal dominant, Autosomal recessive, X-linked recessive
Вік початку
Adolescent, Adult, Childhood, Infancy, Neonatal