Hereditary Coproporphyria Mimicking Guillain-Barré Syndrome After COVID-19 Infection

Hereditary coproporphyria (HCP) is a rare disorder caused by a deficiency of an enzyme, coproporphyrinogen oxidase, in the heme synthetic pathway. This disease has a highly variable clinical presentation with acute attacks of neurologic symptoms that can last from days to months. Rarely, it and othe...

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Detalles Bibliográficos
Autores principales: Upchurch, Margaret, Donnelly, Jonathan P, Deremiah, Emily, Barthol, Colleen, Hafeez, Shaheryar, Anderson, Karl E, Seifi, Ali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873389/
https://www.ncbi.nlm.nih.gov/pubmed/35228944
http://dx.doi.org/10.7759/cureus.21586

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8873389/
https://www.ncbi.nlm.nih.gov/pubmed/35228944
http://dx.doi.org/10.7759/cureus.21586

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