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Hemolytic anemia due to pyrimidine 5' nucleotidase deficiency
rareHemolytic 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.
- Identifiers
- MONDO:0009946 OMIM:266120Orphanet:35120
- 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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