Childhood-Onset Progressive Dystonia With Mitochondrial DNA G14459A Mutation: Efficacy of Long-Term Sodium Succinate Treatment

This article reports the case of an 11-year-old boy with progressive dystonia caused by the homoplasmic G14459A mitochondrial DNA mutation. The patient presented with focal dystonia in the right upper limb at 3 years of age, which progressed over 4 years to exhibit dystonia in both the upper and low...

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Detalles Bibliográficos
Autores principales: Koide, Ayaka, Ozawa, Hiroshi, Kubota, Masaya, Goto, Yuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388318/
https://www.ncbi.nlm.nih.gov/pubmed/28503583
http://dx.doi.org/10.1177/2329048X14550677

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388318/
https://www.ncbi.nlm.nih.gov/pubmed/28503583
http://dx.doi.org/10.1177/2329048X14550677

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