Parkinson disease in Gaucher disease

BACKGROUND: Gaucher disease (GD) is an inborn error of metabolism caused by mutations in the gene (GBA) coding for glucocerebrosidase (GCase), inherited in an autosomal recessive pattern. GD patients have up to 9% risk of developing PD. CASE PRESENTATION: We report two patients with GD that develope...

Descripción completa

Detalles Bibliográficos
Autores principales: Rodriguez-Porcel, Federico, Espay, Alberto J., Carecchio, Miryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440911/
https://www.ncbi.nlm.nih.gov/pubmed/28546865
http://dx.doi.org/10.1186/s40734-017-0054-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440911/
https://www.ncbi.nlm.nih.gov/pubmed/28546865
http://dx.doi.org/10.1186/s40734-017-0054-2

Ejemplares similares