Alternating hemiplegia of childhood

rare

A rare neurodevelopmental disorder characterized by recurrent episodes of hemiplegia and paroxysmal disturbances associated with persistent developmental delay and cognitive impairment.

Identifiers: MONDO:0016241 Orphanet:2131
Part of: Mendelian neurodevelopmental disorder Alternating hemiplegia Hemiplegia
Also known as: adrenal hypoplasia congenita · AHC · alternating hemiplegia · alternating hemiplegia syndrome · childhood alternating hemiplegia

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
X-linked adrenal hypoplasia congenita	MONDO:0010264	1	NR0B1
Alternating hemiplegia of childhood 1	MONDO:0007087		ATP1A2
Alternating hemiplegia of childhood 2	MONDO:0013900

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