Dystonia Responsive to Dopamine: POLG Mutations Should Be Considered If Sensory Neuropathy Is Present

The POLG gene encodes mitochondrial DNA polymerase, and mutations in this gene cause a spectrum of disorders related to mitochondrial DNA depletion or deletion. Dystonia has only rarely been reported as an early and prominent manifestation of POLG mutations. We report a case of a 30-year-old male pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Qiu, Jessica, Kumar, Kishore Raj, Watson, Eloise, Ahmad, Kate, Sue, Carolyn M., Hayes, Michael W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Movement Disorder Society 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175819/
https://www.ncbi.nlm.nih.gov/pubmed/34062649
http://dx.doi.org/10.14802/jmd.20159

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175819/
https://www.ncbi.nlm.nih.gov/pubmed/34062649
http://dx.doi.org/10.14802/jmd.20159

Ejemplares similares