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Синдром арахнодактилії-аномального окостеніння-інтелектуальної недостатності

ORPHA:1129· ICD-10 Q87.8· Arachnodactyly-abnormal ossification-intellectual disability syndrome

Визначення(English summary)

A multiple congenital developmental anomalies syndrome characterized by arachnodactyly of fingers and toes associated with craniofacial dysmorphism (including abnormal cranial ossification, frontal bossing, flat calvaria, shallow deformed orbits resulting in exophtalmos, midface hypoplasia and micrognathia), feeding difficulties in infancy, infantile muscular hypotonia, and developmental delay leading to intellectual disability.

Поширеність
<1 / 1 000 000
Успадкування
Unknown
Вік початку
Infancy, Neonatal