Multiple sclerosis and intracellular cobalamin defect (MMACHC/PRDX1) comorbidity in a young male

BACKGROUND: Methylmalonic acidaemia with homocystinuria type C (cblC defect) is an inherited error of cobalamin metabolism. Cobalamin deficient processing results in high levels of methylmalonic acid and homocysteine. The latter is considered to be a risk factor for multiple sclerosis (MS). We repor...

Descripción completa

Detalles Bibliográficos
Autores principales: Pollini, Luca, Tolve, Manuela, Nardecchia, Francesca, Galosi, Serena, Carducci, Claudia, di Carlo, Emanuele, Carducci, Carla, Leuzzi, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026611/
https://www.ncbi.nlm.nih.gov/pubmed/32099815
http://dx.doi.org/10.1016/j.ymgmr.2019.100560

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026611/
https://www.ncbi.nlm.nih.gov/pubmed/32099815
http://dx.doi.org/10.1016/j.ymgmr.2019.100560

Ejemplares similares