Несиндромальна генетично обумовлена глухота
ORPHA:87884· ICD-10 H90.5· Rare non-syndromic genetic deafness
Визначення(English summary)
Deafness is the most frequent form of sensorial deficit. In the vast majority of cases, the deafness is termed nonsyndromic or isolated and the hearing loss is the only clinical anomaly reported. In developed counties, 60-80% of cases of early-onset hearing loss are of genetic origin.
- Поширеність
- Unknown
- Успадкування
- Autosomal dominant, Autosomal recessive, X-linked recessive
- Вік початку
- Infancy, Neonatal