Bullous skin lesions in a jaundiced infant after phototherapy: a case of congenital erythropoietic porphyria
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Congenital erythropoietic porphyria is a rare autosomal recessive disorder of porphyrin metabolism in which the genetic defect is the deficiency of uroporphyrinogen III cosynthase (UIIIC). Deficiency of this enzyme results in an accumulation of high amounts of... ...
