Hepatoerythropoietic porphyria
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Template:Infobox medical condition (new) Hepatoerythropoietic porphyria is a very rare form of hepatic porphyria caused by a disorder in both genes which code Uroporphyrinogen III decarboxylase (UROD).[1][2]Template:Rp
It has a similar presentation to porphyria cutanea tarda (PCT), but with earlier onset.[3] In classifications which define PCT type 1 as "sporadic" and PCT type 2 as "familial", hepatoerythropoietic porphyria is more similar to type 2.
See also
- Hereditary coproporphyria
- List of cutaneous conditions
- List of dental abnormalities associated with cutaneous conditions
References
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- ↑ "hepatoerythropoietic porphyria" at Dorland's Medical Dictionary
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External links
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