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Синдром глухоти-гіпоплазії емалі-дефектів нігтів

ORPHA:3220· ICD-10 Q82.4· Deafness-enamel hypoplasia-nail defects syndrome

Визначення(English summary)

A rare genetic disease characterized by sensorineural hearing loss, abnormalities in the secondary dentition (such as enamel hypoplasia, taurodontism, or dental overcrowding), and nail abnormalities (including leukonychia and presence of transverse ridges). Association with macular dystrophy has also been reported.

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