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Hyperekplexia-epilepsy syndrome

ORPHA:163985· ICD-10 G25.8

Definition

A rare, X-linked, syndromic intellectual disability disease characterized by neonatal hypertonia which evolves to hypotonia and an exaggerated startle response (to sudden visual, auditory or tactile stimuli), followed by the development of early-onset, frequently refractory, tonic or myoclonic seizures. Progressive epileptic encephalopathy, intellectual disability, and psychomotor development arrest, with subsequent decline, may be additionally associated.

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