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ORPHA:3231· Deafness-onychodystrophy syndrome

Визначення(English summary)

Deafness-onychodystrophy syndrome is a group of rare, genetic, developmental defect during embryogenesis disorders characterized by the association of sensorineural deafness and onychodystrophy (e.g. absent/hypoplastic finger and toenails), as well as brachydactyly and finger-like thumbs. Additional features present in one of the diseases comprising this group include osteodystrophy, intellectual disability, seizures, developmental delay, and distinctive facies.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal dominant, Autosomal recessive
Вік початку
Childhood