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Hepatoerythropoietic porphyria : ウィキペディア英語版
Hepatoerythropoietic porphyria

Hepatoerythropoietic porphyria is a very rare form of hepatic porphyria caused by a disorder in both genes which code Uroporphyrinogen III decarboxylase (UROD).
It has a similar presentation to porphyria cutanea tarda (PCT), but with earlier onset. 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

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Hepatoerythropoietic porphyria」の詳細全文を読む



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