This page was created by volunteers like you!
Help us make it even better. To learn more about contributing to MEpedia, click here.
Join the movement
Visit #MEAction to find support or take action. Donate today to help us improve and expand this project.
Congratulations!
MEpedia has got over 30 million views as of August 2022!

Porphyria

From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history

Poryphyrias are a group of metabolic diseases that are sometimes misdiagnosed as fibromyalgia or multiple chemical sensitivity (MCS).[1][2] Types of porphyrias include:

  • Acute intermittent porphyria
  • ALA-D porphyria
  • Aminolevulinate dehydratase deficiency porphyria
  • Autosomal erythropoietic protoporphyria
  • Congenital erythropoietic porphyria
  • Hepatoerythropoietic porphyria
  • Hereditary coproporphyria
  • Porphyria cutanea tarda
  • Protoporphyria
  • Variegate porphyria[1][3]

Signs and symptoms[edit | edit source]

Treatment[edit | edit source]

ME/CFS[edit | edit source]

Notable articles[edit | edit source]

News articles and interviews[edit | edit source]

See also[edit | edit source]

Learn more[edit | edit source]

References[edit | edit source]

  1. Jump up to: 1.0 1.1 McMillen, Matt. "Porphyria: Types, Symptoms, Causes, and Treatment". WebMD. Retrieved January 7, 2022.
  2. Jump up to: 2.0 2.1 Stölzel, Ulrich; Doss, Manfred O.; Schuppan, Detlef (August 1, 2019). "Clinical Guide and Update on Porphyrias". Gastroenterology. 157 (2): 365–381.e4. doi:10.1053/j.gastro.2019.04.050. ISSN 0016-5085. PMID 31085196.
  3. "Porphyria". NORD (National Organization for Rare Disorders). Retrieved January 7, 2022.