5C58.10Ангилал
Porphyria cutanea tarda
Тодорхойлолт
Porphyria cutanea tarda (PCT) is due to an accumulation of uroporphyrins in plasma from blockage of the normal haem synthetic pathway in the liver at the level of uroporphyrinogen decarboxylase (URO-D). The majority of cases are sporadic and frequently associated with iron overload. PCT manifests as skin fragility and blistering in light-exposed skin, particularly on the dorsa of the hands, together with hypertrichosis.
Индексийн нэр томьёо Index terms · 11
Porphyria cutanea tardaPorphyria, hepatocutaneous typeHeterozygous uroporphyrinogen decarboxylase deficiencyUROD - [uroporphyrinogen decarboxylase] deficiencyPCT - [porphyria cutanea tarda]Sporadic porphyria cutanea tardaSporadic PCT - [porphyria cutanea tarda]Familial porphyria cutanea tardaFamilial PCT - [porphyria cutanea tarda]Toxic porphyria cutanea tardaPorphyria turcica
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