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KDM5C-related syndromic X-linked intellectual disability

ORPHA:85279· ICD-10 Q87.8

Definition

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.

Prevalence
<1 / 1 000 000
Inheritance
X-linked recessive
Age of onset
Childhood