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Синдром Аткіна-Флейца

ORPHA:1193· ICD-10 Q87.8· Atkin-Flaitz syndrome

Визначення(English summary)

A rare X-linked syndromic intellectual disability characterized by variable intellectual deficit, macrocephaly, short stature, and facial dysmorphism (such as prominent forehead, prominent supraorbital ridges, hypertelorism, downslanting palpebral fissures, broad nasal tip, anteverted nostrils, thick lower lip, and localized microdontia). Additional reported features include seizures, post-pubertal macroorchidism, obesity, and short, broad hands with tapered fingers.

Поширеність
<1 / 1 000 000
Успадкування
X-linked dominant
Вік початку
Neonatal