Alternating hemiplegia of childhood 2

Any alternating hemiplegia of childhood in which the cause of the disease is a mutation in the ATP1A3 gene.

Also known as: ATP1A3 alternating hemiplegia of childhood, alternating hemiplegia of childhood 2, alternating hemiplegia of childhood caused by mutation in ATP1A3, alternating hemiplegia of childhood type 2, AHC2

0 clinical trials for this condition and its sub-types.