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...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:Front Neurol
Hlavní autoři: Cordani, Ramona, Stagnaro, Michela, Pisciotta, Livia, Tiziano, Francesco Danilo, Calevo, Maria Grazia, Nobili, Lino, De Grandis, Elisa
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2021
Témata:
Neurology
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8060701/
https://ncbi.nlm.nih.gov/pubmed/33897609
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2021.658451
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky