Contains fulltext : 81557.pdf (publisher's version ) (Closed access)The erythropoietic porphyrias are primarily manifested by skin sensitivity. They are, unlike many other forms of porphyria, usually not associated with neurologic manifestations. Only a few cases have been reported of neuropathy in patients with erythropoietic porphyrias, all characterized by an acute motor and proximally accentuated neuropathy occurring in the setting of hepatic failure. In this report, we present a patient without hepatic failure who presented with a sensorimotor axonal polyneuropathy before being diagnosed with erythropoietic porphyrias. The presented case expands the forms of neurologic complications that can be seen in this specific f...
Background: Acute intermittent porphyria (AIP) is an inherited disorder of heme biosynthesis, the cl...
The acute porphyrias include acute intermittent porphyria (AIP), hereditary coproporphyria and varie...
Porphyrias are a group of congenital and acquired diseases caused by an enzymatic impairment in the ...
The erythropoietic porphyrias are primarily manifested by skin sensitivity. They are, unlike many ot...
The hepatic porphyrias are a group of rare metabolic disorders characterized by enzymatic defects in...
Peripheral neuropathy (PN) has rarely been described as a complication of erythropoietic protoporphy...
The porphyrias are metabolic disorders due to a defect in the heme biosynthetic pathway. Patients ha...
© 2021 Elsevier B.V. All rights reserved.Porphyrias are a set of rare inherited metabolic disorders,...
SummaryBackground and objectivesPorphyrias represent a group of inherited or acquired disorders that...
The porphyrias are inherited metabolic disorders arising from disturbance in the haem biosynthesis p...
Abstract Acute hepatic porphyrias (AHP) can cause severe neurological symptoms involving the central...
Acute hepatic porphyrias (AHP) can cause severe neurological symptoms involving the central, autonom...
Acute intermittent porphyria (AIP) is a rare metabolic disorder characterized by mutations of the po...
SummaryBackground and objectivesPorphyrias represent a group of inherited or acquired disorders that...
The porphyrias are a group of rare metabolic disorders, inherited or acquired, along the heme biosyn...
Background: Acute intermittent porphyria (AIP) is an inherited disorder of heme biosynthesis, the cl...
The acute porphyrias include acute intermittent porphyria (AIP), hereditary coproporphyria and varie...
Porphyrias are a group of congenital and acquired diseases caused by an enzymatic impairment in the ...
The erythropoietic porphyrias are primarily manifested by skin sensitivity. They are, unlike many ot...
The hepatic porphyrias are a group of rare metabolic disorders characterized by enzymatic defects in...
Peripheral neuropathy (PN) has rarely been described as a complication of erythropoietic protoporphy...
The porphyrias are metabolic disorders due to a defect in the heme biosynthetic pathway. Patients ha...
© 2021 Elsevier B.V. All rights reserved.Porphyrias are a set of rare inherited metabolic disorders,...
SummaryBackground and objectivesPorphyrias represent a group of inherited or acquired disorders that...
The porphyrias are inherited metabolic disorders arising from disturbance in the haem biosynthesis p...
Abstract Acute hepatic porphyrias (AHP) can cause severe neurological symptoms involving the central...
Acute hepatic porphyrias (AHP) can cause severe neurological symptoms involving the central, autonom...
Acute intermittent porphyria (AIP) is a rare metabolic disorder characterized by mutations of the po...
SummaryBackground and objectivesPorphyrias represent a group of inherited or acquired disorders that...
The porphyrias are a group of rare metabolic disorders, inherited or acquired, along the heme biosyn...
Background: Acute intermittent porphyria (AIP) is an inherited disorder of heme biosynthesis, the cl...
The acute porphyrias include acute intermittent porphyria (AIP), hereditary coproporphyria and varie...
Porphyrias are a group of congenital and acquired diseases caused by an enzymatic impairment in the ...