enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Hereditary haemochromatosis - Wikipedia

    en.wikipedia.org/wiki/Hereditary_haemochromatosis

    Haemochromatosis is protean in its manifestations, i.e., often presenting with signs or symptoms suggestive of other diagnoses that affect specific organ systems.Many of the signs and symptoms below are uncommon, and most patients with the hereditary form of haemochromatosis do not show any overt signs of disease nor do they have premature morbidity, if they are diagnosed early, but, more ...

  3. Haemochromatosis type 3 - Wikipedia

    en.wikipedia.org/wiki/Haemochromatosis_type_3

    Majority of the cases of hemochromatosis are caused by mutations in the HFE (Homeostatic Iron Regulator) gene. [17] Type 3 HH is characterized by compound heterozygote mutations in both transferrin receptor 2 (TFR2) and HFE, i.e. a single mutation in each gene. HFE is located on chromosome 6 and TFR2 is located on chromosome 7.

  4. HFE H63D gene mutation - Wikipedia

    en.wikipedia.org/wiki/HFE_H63D_gene_mutation

    This mutation is associated with diverse health issues, however H63D syndrome is the only known specific expression of a homozygous HFE-H63D mutation to date. The homozygous HFE-H63D mutation is the cause of classic and treatable hemochromatosis in only 6.7% of its carriers. [25] H63D syndrome is independently a distinct entity, and the ...

  5. HFE (gene) - Wikipedia

    en.wikipedia.org/wiki/HFE_(gene)

    The protein encoded by this gene is an integral membrane protein that is similar to MHC class I-type proteins and associates with beta-2 microglobulin (beta2M). It is thought that this protein functions to regulate circulating iron uptake by regulating the interaction of the transferrin receptor with transferrin.

  6. Iron overload - Wikipedia

    en.wikipedia.org/wiki/Iron_overload

    Iron overload (also known as haemochromatosis or hemochromatosis) is the abnormal and increased accumulation of total iron in the body, leading to organ damage. [1] The primary mechanism of organ damage is oxidative stress, as elevated intracellular iron levels increase free radical formation via the Fenton reaction.

  7. Hemojuvelin - Wikipedia

    en.wikipedia.org/wiki/Hemojuvelin

    Hemojuvelin (HJV), also known as repulsive guidance molecule C (RGMc) or hemochromatosis type 2 protein (HFE2), is a membrane-bound and soluble protein in mammals that is responsible for the iron overload condition known as juvenile hemochromatosis in humans, a severe form of hemochromatosis.

  8. HFE - Wikipedia

    en.wikipedia.org/wiki/HFE

    HFE (gene), a gene that encodes the Human hemochromatosis protein; Hello from Earth, an interstellar radio message; Hidden Field Equations, a cryptosystem; H-parameter model (h FE), the current gain of a bipolar junction transistor; Human factors engineering; Hydrofluoroether, a solvent

  9. Variegate porphyria - Wikipedia

    en.wikipedia.org/wiki/Variegate_porphyria

    An additional aggravating mutation affecting variegate porphyria can be found at 6p21.3 on the HFE gene. [7] A 2006 clinical, biochemical and mutational study of eight Swiss variegate porphyria patients and their families found four novel PPOX gene mutations believed to be unique to the Swiss population. [8]

  1. Related searches hfe mutation wikipedia tieng viet kyuranger youtube free video on full body stretch

    hfe mutation wikipediahfe mutations in liver
    hfe gene mutationhfe genetic model
    hfe h63d mutationh63d mutation