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  • Title: [Porphyria cutanea tarda in a 4-year-old child with uroporphyrinogen decarboxylase deficiency].
    Author: Cotton JB, Abeille A, Jeune R, Ladreyt-Ponchon JP, Grenier JL.
    Journal: Pediatrie; 1986 Dec; 41(8):617-27. PubMed ID: 3575073.
    Abstract:
    A 4 years old girl presents a typical case of patent form of cutaneous late porphyria with a reduced activity of the erythrocyte, uroporphyrinogen decarboxylase (UROD) genetically transmitted over 3 generations; a multifactor inheritance (HLA A3, a normal phenotype of alpha 1 antitrypsin, exogenous toxins, or viral infections) is discussed.
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