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...

Descripción completa

Detalles Bibliográficos
Autores principales: Cordani, Ramona, Stagnaro, Michela, Pisciotta, Livia, Tiziano, Francesco Danilo, Calevo, Maria Grazia, Nobili, Lino, De Grandis, Elisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060701/
https://www.ncbi.nlm.nih.gov/pubmed/33897609
http://dx.doi.org/10.3389/fneur.2021.658451

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060701/
https://www.ncbi.nlm.nih.gov/pubmed/33897609
http://dx.doi.org/10.3389/fneur.2021.658451

Ejemplares similares