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Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency

rare

Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency is a rare, hereditary, hemolytic anemia due to an erythrocyte nucleotide metabolism disorder characterized by mild to moderate hemolytic anemia associated with basophilic stippling and the accumulation of high concentrations of pyrimidine nucleotides within the erythrocyte. Patients present with variable features of jaundice, splenomegaly, hepatomegaly, gallstones, and sometimes require transfusions. Rare cases of mild development delay and learning difficulties are reported.

Causal genes
NT5C3A
Also known as
anemia, congenital, nonspherocytic hemolytic, 8 · anemia, hemolytic, due to UMPH1 deficiency · hemolytic anaemia due to P5N deficiency · hemolytic anaemia due to UMPH1 deficiency · hemolytic anemia due to P5N deficiency

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