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  2. Severe congenital neutropenia - Wikipedia

    en.wikipedia.org/wiki/Severe_Congenital_Neutropenia

    Severe congenital neutropenia (SCN), also often known as Kostmann syndrome or disease, is a group of rare disorders that affect myelopoiesis, causing a congenital form of neutropenia, usually without other physical malformations. SCN manifests in infancy with life-threatening bacterial infections. [2]

  3. List of ICD-9 codes 760–779: certain conditions originating ...

    en.wikipedia.org/wiki/List_of_ICD-9_codes_760...

    This is a shortened version of the fifteenth chapter of the ICD-9: Certain Conditions originating in the Perinatal Period. It covers ICD codes 760 to 779. The full chapter can be found on pages 439 to 453 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1.

  4. Neutropenia - Wikipedia

    en.wikipedia.org/wiki/Neutropenia

    The congenital neutropenia (severe and cyclic type) is autosomal dominant, with mutations in the ELA2 gene (neutrophil elastase) as the most common genetic reason for this condition. [7] Acquired neutropenia (immune-associated neutropenia) is due to anti-neutrophil antibodies that target neutrophil-specific antigens , ultimately altering ...

  5. List of primary immunodeficiencies - Wikipedia

    en.wikipedia.org/wiki/List_of_primary_immuno...

    Severe Congenital Neutropenia: due to ELA2 deficiency (with myelodysplasia) Severe Congenital Neutropenia: due to GFI1 deficiency (with T/B lymphopenia) Elastase deficiency; Kostmann syndrome (HAX1 deficiency) Neutropenia with cardiac and urogenital malformations; Glycogen storage disease type 1b; Cohen syndrome; Clericuzio syndrome; Cyclic ...

  6. Cyclic neutropenia - Wikipedia

    en.wikipedia.org/wiki/Cyclic_neutropenia

    Cyclic neutropenia (CyN), like severe congenital neutropenia (SCN), is a rare disorder. It is considered that in the general population, CyN has a frequency of one in one million. [ 1 ] It is the result of autosomal dominant mutation in ELANE gene located on the short arm (p) of chromosome 19 (19p13.3), the gene encoding neutrophil elastase ...

  7. Myelokathexis - Wikipedia

    en.wikipedia.org/wiki/Myelokathexis

    Myelokathexis is a congenital disorder of the white blood cells that causes severe, chronic leukopenia (a reduction of circulating white blood cells) and neutropenia (a reduction of neutrophil granulocytes). [1] The disorder is believed to be inherited in an autosomal dominant manner.

  8. List of ICD-9 codes 280–289: diseases of the blood and blood ...

    en.wikipedia.org/wiki/List_of_ICD-9_codes_280...

    This is a shortened version of the fourth chapter of the ICD-9: Diseases of the Blood and Blood-forming Organs. It covers ICD codes 280 to 289. The full chapter can be found on pages 167 to 175 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1.

  9. Leukopenia - Wikipedia

    en.wikipedia.org/wiki/Leukopenia

    Neutropenia, a subtype of leukopenia, refers to a decrease in the number of circulating neutrophil granulocytes, the most abundant white blood cells. The terms leukopenia and neutropenia may occasionally be used interchangeably, as the neutrophil count is the most important indicator of infection risk. Agranulocytosis is an acute form of ...