Английская Википедия:Hepatoerythropoietic porphyria

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Шаблон: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]Шаблон: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

References

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External links

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Шаблон:Heme metabolism disorders


Шаблон:Endocrine-disease-stub