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Синдром глухоти-інтелектуальної недостатності, тип Мартіна-Пробста

ORPHA:85321· ICD-10 Q87.8· Deafness-intellectual disability syndrome, Martin-Probst type

Визначення(English summary)

A rare X-linked syndromic intellectual disability characterized by congenital sensorineural hearing loss, varying degrees of intellectual disability, short stature, and dysmorphic facial features (such as telecanthus, epicanthic folds, broad nasal root, malar hypoplasia, low-set ears, dental anomalies, and micrognathia). Additional reported manifestations include microcephaly, renal and genitourinary abnormalities, widely spaced, hypoplastic nipples, and adult onset of progressive pancytopenia.

Поширеність
<1 / 1 000 000
Успадкування
X-linked recessive
Вік початку
Infancy, Neonatal