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  2. Polycythemia - Wikipedia

    en.wikipedia.org/wiki/Polycythemia

    Chuvash erythrocytosis or Chuvash polycythemia is an autosomal recessive form of erythrocytosis endemic in patients from the Chuvash Republic in Russia. Chuvash erythrocytosis is associated with homozygosity for a C598T mutation in the von Hippel–Lindau gene ( VHL ), which is needed for the destruction of hypoxia-inducible factors in the ...

  3. Myomatous erythrocytosis syndrome - Wikipedia

    en.wikipedia.org/wiki/Myomatous_erythrocytosis...

    Myomatous erythrocytosis syndrome (MES) is an uncommon gynecological disorder associated with isolated polycythemia and uterine fibroids. The primary feature of myomatous erythrocytosis syndrome is that hemoglobin goes back to its baseline level following the removal of the myoma .

  4. Polycythemia vera - Wikipedia

    en.wikipedia.org/wiki/Polycythemia_vera

    In oncology, polycythemia vera (PV) is an uncommon myeloproliferative neoplasm in which the bone marrow makes too many red blood cells. [1] The majority of cases [2] are caused by mutations in the JAK2 gene, most commonly resulting in a single amino acid change in its protein product from valine to phenylalanine at position 617.

  5. Erythrocytosis - Wikipedia

    en.wikipedia.org/?title=Erythrocytosis&redirect=no

    This page was last edited on 13 November 2006, at 03:38 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  6. TEMPI syndrome - Wikipedia

    en.wikipedia.org/wiki/Tempi_syndrome

    Telangiectasia-erythrocytosis-monoclonal gammopathy-perinephric-fluid collections-intrapulmonary shunting syndrome TEMPI syndrome is an orphan disease where the patients share five characteristics from which the acronym is derived: telangiectasias , elevated erythropoietin and erythrocytosis , monoclonal gammopathy , perinephric fluid ...

  7. Hemolytic disease of the newborn - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_disease_of_the...

    Hemolytic disease of the newborn, also known as hemolytic disease of the fetus and newborn, HDN, HDFN, or erythroblastosis fetalis, [1] [2] is an alloimmune condition that develops in a fetus at or around birth, when the IgG molecules (one of the five main types of antibodies) produced by the mother pass through the placenta.

  8. Hematologic disease - Wikipedia

    en.wikipedia.org/wiki/Hematologic_disease

    Erythrocytosis (increase in the number of red blood cells) Leukocytosis (increase in the number of white blood cells) Thrombocytosis (increase in the number of platelets) Myeloproliferative disorder; Transient myeloproliferative disease; Coagulopathies (disorders of bleeding and coagulation) Thrombocytosis; Recurrent thrombosis

  9. Cytosis - Wikipedia

    en.wikipedia.org/wiki/Cytosis

    Pinocytosis, also known as cell drinking, is the absorption of small aqueous particles along with the membrane receptors that recognize them.It is an example of fluid phase endocytosis and is usually a continuous process within the cell.