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X-linked dyserythropoetic anemia with abnormal platelets and neutropenia

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Description

XLANP is an X-linked recessive hematologic disorder characterized by early-onset anemia and bone marrow erythroid hypoplasia with variable neutropenia. Some patients may have low platelets or platelet abnormalities. The severity is variable. Some patients have shown a favorable response to corticosteroid treatment (summary by Hollanda et al., 2006 and Sankaran et al., 2012). In some cases, the disorder may resemble Diamond-Blackfan anemia (see, e.g., DBA1; 105650) (Sankaran et al., 2012; Parrella et al., 2014; Klar et al., 2014).

OMIM

  • Mode of Inheritance

  • X-linked recessive inheritance

VARIANTS

3

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Genes

External Links

  • OMIM

    300835

  • Orphanet

    363727

  • HPO
  • Medgen

    C3550856

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