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CLCN4-related X-linked intellectual disability syndrome

ORPHA:485350· ICD-10 F78.1

Definition

A rare X-linked syndromic intellectual disability characterized by intellectual disability of variable degree, behavioral anomalies (including autism, mood disorders, obsessive-compulsive behavior, and hetero- and auto-aggression), and epilepsy. Progressive neurological symptoms like movement disorders and spasticity, as well as subtle dysmorphic features have also been reported. Heterozygous females may be as severely affected as males.

Prevalence
<1 / 1 000 000
Inheritance
X-linked dominant
Age of onset
Childhood, Infancy