vitalwiki

Інтелектуальна недостатність-хондродисплазія, повязані з QRICH1

ORPHA:580940· ICD-10 Q87.8· QRICH1-related intellectual disability-chondrodysplasia syndrome

Визначення(English summary)

A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by the association of developmental delay and mild chondrodysplasia with short stature and abnormal growth plate morphology. Dysmorphic facial features are variable and may include hypertelorism, upslanting palpebral fissures, broad nose with broad nasal tip, and low-set, cup-shaped ears, among others. Autism spectrum disorder and neurologic abnormalities have also been reported.

Поширеність
<1 / 1 000 000
Успадкування
Autosomal dominant
Вік початку
Antenatal, Infancy, Neonatal