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  2. Hereditary haemochromatosis - Wikipedia

    en.wikipedia.org/wiki/Hereditary_haemochromatosis

    A study of 3,011 unrelated white Australians found that 14% were heterozygous carriers of an HFE mutation, 0.5% were homozygous for an HFE mutation, and only 0.25% of the study population had clinically relevant iron overload. Most patients who are homozygous for HFE mutations do not manifest clinically relevant haemochromatosis (see Genetics ...

  3. HFE (gene) - Wikipedia

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

    At least 42 mutations involving HFE introns and exons have been discovered, most of them in persons with hemochromatosis or their family members. [25] Most of these mutations are rare. Many of the mutations cause or probably cause hemochromatosis phenotypes, often in compound heterozygosity with HFE C282Y.

  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. 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.

  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. Uchu Sentai Kyuranger - Wikipedia

    en.wikipedia.org/wiki/Uchu_Sentai_Kyuranger

    Uchu Sentai Kyuranger: Transformation Lessons ~Let's Star Change Together!~ (宇宙戦隊キュウレンジャー 変身講座 ~君も一緒にスターチェンジ!~, Uchū Sentai Kyūrenjā Henshin Kōza Kimi mo Issho no Sutā Chenji!) is a web-exclusive series released on Toei's official YouTube channel. It accompanies the airing of ...

  8. Compound heterozygosity - Wikipedia

    en.wikipedia.org/wiki/Compound_heterozygosity

    Clinically, most cases of hemochromatosis are found in homozygotes for the most common mutation in the HFE gene. [1] But at each gene locus associated with the disease, there is the possibility of compound heterozygosity, often caused by inheritance of two unrelated alleles, of which one is a common or classic mutation, while the other is a ...

  9. Lupinranger VS Patranger VS Kyuranger - Wikipedia

    en.wikipedia.org/wiki/Lupinranger_VS_Patranger...

    Concurrently, Kyuranger members Stinger, Hammie, and Spada search for Lucky, but track Minato's guitar to a warehouse, where the Lupinrangers and BN thieves learn that Lipig is working with Don Arkage, who intends to use the Hyper Planedium in Minato's guitar to become invincible. The Lupinrangers and Kyurangers confront the two and defeat ...