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X-linked intellectual disability, Cabezas type

ORPHA:85293· ICD-10 Q87.8

Definition

An X-linked syndromic intellectual disability characterized by developmental delay, intellectual disability (ID) with severe speech impairment, and short stature. Variable additional clinical features have been associated, including behavioral disturbances, gait abnormalities, tremor, seizures, hypogonadism, truncal obesity, unspecific facial dysmorphism, and small hands and feet.

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