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Синдром Мора-Транебєрга

ORPHA:52368· ICD-10 E88.8· Mohr-Tranebjaerg syndrome

Визначення(English summary)

A rare X-linked syndromic intellectual disability characterized by clinical manifestations commencing with early childhood onset hearing loss, followed by adolescent onset progressive dystonia or ataxia, visual impairment from early adulthood onwards and dementia from the 4th decade onwards.

Поширеність
<1 / 1 000 000
Успадкування
X-linked recessive
Вік початку
Childhood