Hereditary Spastic Paraplegia Is a Common Phenotypic Finding in ARG1 Deficiency, P5CS Deficiency and HHH Syndrome: Three Inborn Errors of Metabolism Caused by Alteration of an Interconnected Pathway of Glutamate and Urea Cycle Metabolism

Hereditary Spastic Paraplegias (HSPs) are a clinically and genetically heterogeneous group of neurodegenerative disorders characterized by a progressive rigidity and weakness of the lower limbs, caused by pyramidal tract lesions. As of today, 80 different forms of HSP have been mapped, 64 genes have...

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Detalles Bibliográficos
Autores principales: Panza, Emanuele, Martinelli, Diego, Magini, Pamela, Dionisi Vici, Carlo, Seri, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395431/
https://www.ncbi.nlm.nih.gov/pubmed/30853934
http://dx.doi.org/10.3389/fneur.2019.00131

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6395431/
https://www.ncbi.nlm.nih.gov/pubmed/30853934
http://dx.doi.org/10.3389/fneur.2019.00131

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