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Синдромна Х-зчеплена інтелектуальна недостатність, повязана з KDM5C

ORPHA:85279· ICD-10 Q87.8· KDM5C-related syndromic X-linked intellectual disability

Визначення(English summary)

A rare multiple congenital anomalies/dysmorphic syndrome characterized by mild to severe intellectual deficit associated with variable clinical manifestations including spasticity, cryptorchidism, maxillary hypoplasia, alopecia areata, epilepsy, short stature, impaired speech, and behavioral problems.

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