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Alternating hemiplegia of childhood

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Name:
Alternating hemiplegia of childhood
Description:
A rare, genetic, neurodevelopmental disorder characterized by early-onset of recurrent, transient episodes of hemiplegia (including quadriplegia), which typically disappear upon sleep.
ORPHAcode:
2131
Synonyms:
AHC
XREF(s):
Orphanet
MeSH
ICD-10
OMIM
OMIM
Analyte(s):
CACNA1A
ATP1A2
ATP1A3
SLC1A3
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14