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单词 Familial porphyria cutanea tarda
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Familial porphyria cutanea tarda

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Porphyria cutanea tarda

The reaction catalyzed by UroD
20% of cases of porphyria cutanea tarda are inherited in an autosomal dominant pattern.

Porphyria cutanea tarda (PCT) is the most common subtype of porphyria. The disease is named because it is a porphyria that often presents with skin manifestations later in life. The disorder results from low levels of the enzyme responsible for the fifth step in heme production. Heme is a vital molecule for all of the body's organs. It is a component of hemoglobin, the molecule that carries oxygen in the blood.

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