More Than a Decade of Misdiagnosis of Alternating Hemiplegia of Childhood with Catastrophic Outcome

Alternating hemiplegia of childhood (AHC) is a distinct clinical disorder characterized by recurrent episodes of hemiplegia, abnormal ocular movement, and progressive developmental delay. It is an extremely rare genetic disorder related to ATP1A3 gene mutations. In this paper, we present a case of A...

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Detalles Bibliográficos
Autores principales: Algahtani, Hussein, Ibrahim, Bashair, Shirah, Bader, Aldarmahi, Ahmad, Abdullah, Ahad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576389/
https://www.ncbi.nlm.nih.gov/pubmed/28900444
http://dx.doi.org/10.1155/2017/5769837

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5576389/
https://www.ncbi.nlm.nih.gov/pubmed/28900444
http://dx.doi.org/10.1155/2017/5769837

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