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Alternating hemiplegia of childhood 2
- ... mutation leads to the specific features of alternating hemiplegia of childhood. More About This Health Condition More than 30 mutations in the ATP1A2 gene have been identified in people with familial hemiplegic migraine type 2 (FHM2). This condition is characterized by migraine headaches ...
- ... primary cause of a neurological condition called alternating hemiplegia of childhood. This condition is characterized by recurrent episodes of ... time. Most ATP1A3 gene variants associated with alternating hemiplegia of childhood change single protein building blocks (amino acids) in ...
