porphyria cutanea tarda hereditaria
por·phyr·i·a cu·ta·ne·a tar·da (PCT),[MIM*176090, MIM*176100]
familial or sporadic porphyria characterized by liver dysfunction and photosensitive cutaneous lesions, with bullae, hyperpigmentation, and sclerodermalike changes in the skin and increased excretion of uroporphyrin; caused by a deficiency of uroporphyrinogen decarboxylase induced in sporadic cases by chronic alcoholism; autosomal dominant inheritance in familial cases.
Synonym(s): symptomatic porphyria
porphyria cutanea tarda hereditaria(1) Porphyria cutanea tarda, see there.
(2) Variegate porphyria.