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Diamond-Blackfan anemia

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Description

Diamond-Blackfan anemia (DBA) is characterized by a profound normochromic and usually macrocytic anemia with normal leukocytes and platelets, congenital malformations in up to 50%, and growth deficiency in 30% of affected individuals. The hematologic complications occur in 90% of affected individuals during the first year of life. The phenotypic spectrum ranges from a mild form (e.g., mild anemia or no anemia with only subtle erythroid abnormalities, physical malformations without anemia) to a severe form of fetal anemia resulting in nonimmune hydrops fetalis. DBA is associated with an increased risk for acute myelogenous leukemia (AML), myelodysplastic syndrome (MDS), and solid tumors including osteogenic sarcoma.

GeneReviews

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

215

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Genes

External Links

  • OMIM
  • Orphanet

    124

  • HPO

    3307

  • Medgen

    C1260899

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