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  2. Hereditary haemochromatosis - Wikipedia

    en.wikipedia.org/wiki/Hereditary_haemochromatosis

    There are five types of hereditary hemochromatosis: type 1, 2 (2A, 2B), 3, 4 [9] and 5, [10] all caused by mutated genes. Hereditary hemochromatosis type 1 is the most frequent, and uniquely related to the HFE gene. It is most common among those of Northern European ancestry, in particular those of Celtic descent. [11]

  3. HFE H63D gene mutation - Wikipedia

    en.wikipedia.org/wiki/HFE_H63D_gene_mutation

    The HFE H63D is a single-nucleotide polymorphism in the HFE gene (c.187C>G, rs1799945), which results in the substitution of a histidine for an aspartic acid at amino acid position 63 of the HFE protein (p.His63Asp). HFE participates in the regulation of iron absorption. [1] [2] [3] Homozygous H63D variant can occasionally be the cause of ...

  4. 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.

  5. HFE (gene) - Wikipedia

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

    Mice homozygous for this deletion also had increased duodenal iron absorption, elevated plasma iron and transferrin saturation levels, and iron overload, mainly in hepatocytes. [30] Mice have also been created that are homozygous for a missense mutation in Hfe (C282Y). These mice correspond to humans with hemochromatosis who are homozygous for ...

  6. Hemochromatosis type 4 - Wikipedia

    en.wikipedia.org/wiki/Hemochromatosis_type_4

    Diagnosis is based upon identification of symptoms, medical history, family history, and laboratory tests. Blood tests may show high levels of ferritin and low, normal, or high levels of transferrin saturation, depending on the form of hemochromatosis. The diagnosis must be confirmed by genetic testing for SLC40A1 mutations. [14]

  7. Sisters Who Had Heart Transplants 7 Years Apart Celebrate ...

    www.aol.com/sisters-had-heart-transplants-7...

    Two sisters were diagnosed with the same genetic heart condition 7 years apart, and both ended up getting heart transplants at 38 years old

  8. The NBA has a 'missing stars' problem with injuries piling up ...

    www.aol.com/sports/nba-missing-stars-problem...

    That’s a 35% surge from last season and up 16% from 2023-24’s level, according to Stotts’ data provided to Yahoo Sports. Either way you look at it, star absences and overall games lost due ...

  9. Moment Tiny Abused Parrot Snuggles Into Rescuer's Palm in ...

    www.aol.com/lifestyle/moment-tiny-abused-parrot...

    This anti-aging eye gel is a must-have for winter — and it's 20% off right now