Acute Hepatic Porphyrias: Review and Recent Progress

The acute hepatic porphyrias (AHPs) are a group of four inherited diseases of heme biosynthesis that present with episodic, acute neurovisceral symptoms. The four types are 5‐aminolevulinic acid (ALA) dehydratase deficiency porphyria, acute intermittent porphyria, hereditary coproporphyria, and vari...

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Detalles Bibliográficos
Autores principales: Wang, Bruce, Rudnick, Sean, Cengia, Brent, Bonkovsky, Herbert L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357830/
https://www.ncbi.nlm.nih.gov/pubmed/30766957
http://dx.doi.org/10.1002/hep4.1297

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357830/
https://www.ncbi.nlm.nih.gov/pubmed/30766957
http://dx.doi.org/10.1002/hep4.1297

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