Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia

BACKGROUND: Hyperornithinemia–hyperammonemia–homocitrullinuria (HHH) syndrome is a rare disorder of urea cycle characterized by progressive pyramidal and cerebellar dysfunction, whose pathophysiology is not yet fully understood. Here we describe the spectrum of the long fibers involvement in HHH syn...

Descripción completa

Detalles Bibliográficos
Autores principales: Olivieri, Giorgia, Pro, Stefano, Diodato, Daria, Di Capua, Matteo, Longo, Daniela, Martinelli, Diego, Bertini, Enrico, Dionisi-Vici, Carlo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708179/
https://www.ncbi.nlm.nih.gov/pubmed/31443672
http://dx.doi.org/10.1186/s13023-019-1181-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6708179/
https://www.ncbi.nlm.nih.gov/pubmed/31443672
http://dx.doi.org/10.1186/s13023-019-1181-7

Ejemplares similares