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Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia

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Description

Combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia is an inborn error of folate metabolism due to deficiency of methylenetetrahydrofolate dehydrogenase-1. Manifestations may include hemolytic uremic syndrome, macrocytosis, epilepsy, hearing loss, retinopathy, mild mental retardation, lymphopenia involving all subsets, and low T-cell receptor excision circles. Folinic acid supplementation is an effective treatment (summary by Ramakrishnan et al., 2016).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

13

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Genes

External Links

  • OMIM

    617780

  • Orphanet
  • HPO
  • Medgen

    C4540434

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