Alternating Hemiplegia of Childhood: Genotype–Phenotype Correlations in a Cohort of 39 Italian Patients

Alternating Hemiplegia of Childhood: Genotype–Phenotype Correlations in a Cohort of 39 Italian Patients

Alternating hemiplegia of childhood is a rare neurological disease characterized by paroxysmal movement disorders and chronic neurological disturbances, with onset before 18 months of age. Mutations in the ATP1A3 gene have been identified in up to 80% of patients. Thirty-nine patients [20 females, 1...

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Bibliographic Details
Main Authors: Ramona Cordani, Michela Stagnaro, Livia Pisciotta, Francesco Danilo Tiziano, Maria Grazia Calevo, Lino Nobili, I.B.AHC Consortium, Elisa De Grandis
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-04-01
Series:Frontiers in Neurology
Subjects:
alternating hemiplegia of childhood
ATP1A3
movement disorder
genotype
phenotype
flunarizine
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2021.658451/full

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https://www.frontiersin.org/articles/10.3389/fneur.2021.658451/full

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