Acute Hepatic Porphyria: Pathophysiological Basis of Neuromuscular Manifestations

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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Bibliographic Details
Main Authors: Paulo Victor Sgobbi de Souza, Bruno de Mattos Lombardi Badia, Igor Braga Farias, Wladimir Bocca Vieira de Rezende Pinto, Acary Souza Bulle Oliveira
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-09-01
Series:Frontiers in Neuroscience
Subjects:
acute hepatic porphyria
neuromuscular
neuropathy
rhabdomyolysis
dysautonomia
pathophysiology
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2021.715523/full

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https://www.frontiersin.org/articles/10.3389/fnins.2021.715523/full

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