Acute Hepatic Porphyria: Pathophysiological Basis of Neuromuscular Manifestations

Acute hepatic porphyria represents a rare, underdiagnosed group of inherited metabolic disorders due to hereditary defects of heme group biosynthesis pathway. Most patients have their definite diagnosis after several years of complex and disabling clinical manifestations and commonly after life-thre...

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Detalles Bibliográficos
Autores principales: de Souza, Paulo Victor Sgobbi, Badia, Bruno de Mattos Lombardi, Farias, Igor Braga, Pinto, Wladimir Bocca Vieira de Rezende, Oliveira, Acary Souza Bulle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502968/
https://www.ncbi.nlm.nih.gov/pubmed/34646118
http://dx.doi.org/10.3389/fnins.2021.715523

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502968/
https://www.ncbi.nlm.nih.gov/pubmed/34646118
http://dx.doi.org/10.3389/fnins.2021.715523

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