Acute porphyrias – A neurological perspective
Abstract Acute hepatic porphyrias (AHP) can cause severe neurological symptoms involving the central, autonomic, and peripheral nervous system. Due to their relative rarity and their chameleon‐like presentation, delayed diagnosis and misdiagnosis are common. AHPs are genetically inherited disorders...
Saved in:
Main Authors: | Lea M. Gerischer, Franziska Scheibe, Astrid Nümann, Martin Köhnlein, Ulrich Stölzel, Andreas Meisel |
---|---|
Format: | article |
Language: | EN |
Published: |
Wiley
2021
|
Subjects: | |
Online Access: | https://doaj.org/article/f34b13f667764ceabf9929202318d941 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Encefalopatía posterior reversible como primera manifestación del Síndrome de Guillain-Barré
by: Urrutia L,Sergio, et al.
Published: (2012) -
Síndrome anti-GQ1b: Descripción de cuatro pacientes y revisión de la literatura
by: Uribe S.M,Reinaldo, et al.
Published: (2013) -
Muerte encefálica: la necesidad de una causa suficiente y necesaria: A propósito de un caso de deseferentación completa por síndrome de Guillain Barré
by: Sáez M,David, et al.
Published: (2011) -
An Atypical Case of Congenital Erythropoietic Porphyria
by: Bénédicte Sudrié-Arnaud, et al.
Published: (2021) -
Síndrome de Guillain-Barre y Strohl, Forma Landry: Manejo con respirador mecánico
by: Samuel F,García, et al.
Published: (1977)