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3 Possible Causes for Neonatal Hemolytic Anemia (Harderoporphyria

  • Hereditary Coproporphyria

    In such patients the presence of a specific mutation (K404E) on one or both alleles produces a neonatal hemolytic anemia that is known as "harderoporphyria"; mutations on[ncbi.nlm.nih.gov] Here, we describe a Turkish male infant, the product of a consanguineous union, who presented with the Harderoporphyria phenotype including neonatal hyperbilirubinemia, hemolytic[doi.org] anemia, hepatosplenomegaly, and skin lesions when exposed to UV light.[doi.org]

  • Erythropoietic Coproporphyria

    hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basis.[academic.oup.com] Harderoporphyria is a rare erythropoietic variant form of HCP, characterized by neonatal hemolytic anemia, sometimes accompanied by skin lesions and accumulation of harderoporphyrin[academic.oup.com] 278. 11 Lamoril, J., Puy, H., Gouya, L., Rosipal, R., Da Silva, V., Grandchamp, B., Foint, T., Bader-Meunier, B., Dommergues, J.P., Deybach, J.C. and Nordmann, Y. ( 1998 ) Neonatal[academic.oup.com]

  • Hepatoerythropoietic Porphyria

    Harderoporphyria is a rare homozygous erythropoietic variant form of HCP, characterized by neonatal hemolytic anemia, sometimes accompanied by skin lesions, and massive excretion[mendelian.co]

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