About Porphyria
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Porphyria is not a single disease but a group of at least eight disorders that differ considerably from each other. A common feature in all porphyrias is the accumulation in the body of porphyrins or porphyrin precursors. Although these are normal body chemicals, they normally do not accumulate. Precisely which of these chemicals builds up depends on the type of porphyria.
The terms porphyrin and porphyria are derived from the Greek word porphyrus, meaning purple. Urine from some porphyria patients may be reddish in color due to the presence of excess porphyrins and related substances in the urine, and the urine may darken after exposure to light.
The symptoms and treatment vary significantly from one type of Porphyria to the next.
Porphyria symptoms arise mostly from effects on either the nervous system or the skin. Effects on the nervous system occur in the acute porphyrias (AIP, ADP, HCP and VP). Proper diagnosis is often delayed because the symptoms are nonspecific. Skin manifestations can include burning, blistering and scarring of sun-exposed areas.
This section of our website includes basic information about symptoms, diagnosis and treatment of the eight types of Porphyria. You will also find information on diet and nutrition in porphyria and on the history of the disease.
Please see the Testing for Porphyria, Treatment Options and Healthcare Professionals sections of our website for more detailed information.
- About the APF
- About Porphyria
- Acute Intermittent Porphyria (AIP)
- Variegate Porphyria (VP)
- Hereditary Coproporphyria (HCP)
- ALAD Porphyria (ADP)
- Porphyria Cutanea Tarda (PCT)
- Erythropoietic Protoporphyria (EPP) or Protoporphyria
- Congenital Erythropoietic Porphyria (CEP)
- Hepatoerythropoietic Porphyria (HEP)
- Diet and Nutrition
- History of Porphyria
- Testing for Porphyria
- Treatment
- Get Involved
- For Healthcare Professionals
- News
- Additional Resources
- Donate


