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- W2029596704 abstract "Cutaneous fragility at age 2 years with blistering, scarring, milia, and hypertrichosis at age 4 years were noted in an otherwise healthy girl who had no family history of porphyria. Results of porphyrin analyses of urine, serum, and red blood cells revealed a pattern consistent with porphyria cutanea tarda. Red blood cell uroporphyrinogen decarboxylase activity was diminished to approximately 50% of normal in the child and in her mother and maternal grandmother, who were without symptoms; activity was normal in her sister, father, and maternal grandfather. Therapeutic phlebotomies were followed by a biochemical and clinical remission." @default.
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- W2029596704 date "1998-09-01" @default.
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- W2029596704 title "Nodular focal fatty infiltration of the liver in porphyria cutanea tarda" @default.
- W2029596704 doi "https://doi.org/10.1016/s0926-9959(98)95636-7" @default.
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