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40 Possible Causes for Chronic Fatigue Syndrome, Mutation in the Hereditary Hemochromatosis Gene

  • Hemochromatosis

    Hereditary hemochromatosis can be divided into HFE- and non-HFE-related based on genetic mutations in different genes.[ncbi.nlm.nih.gov] Gene mutations that cause hemochromatosis A gene called HFE is most often the cause of hereditary hemochromatosis. You inherit one HFE gene from each of your parents.[mayoclinic.com] Sanger sequencing was conducted for the screening of mutation in the hereditary hemochromatosis related genes.[ncbi.nlm.nih.gov]

  • Congestive Heart Failure

    The actuarial survival rates of persons who are homozygous for the mutation of the hemochromatosis gene C282Y have been reported to be 95%, 93%, and 66%, at 5, 10, and 20[doi.org] Health status in patients with chronic fatigue syndrome and in general population and disease comparison groups. Am J Med 1996 ; 101 : 281 –90.[doi.org] Types of participants Adult participants with chronic heart failure, defined as a clinical syndrome characterised by breathlessness and fatigue that is caused by an inability[doi.org]

  • Behçet Disease

    OBJECTIVE: The aim of this work was to establish human leukocyte antigen (HLA) class I and hereditary hemochromatosis gene (HFE) mutation associations with recurrent aphthous[ncbi.nlm.nih.gov]

  • Iron Deficiency

    These can include, chronic fatigue, weakness, dizziness, headaches, depression, sore tongue, sensitivity to cold (low body temp), shortness of breath doing simple tasks (climbing[irondisorders.org] A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet. 1996;13:399–408. PubMed CrossRef Google Scholar 8.[doi.org] A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nat Genet. 1996; 13 :399–408. [ PubMed ] [ Google Scholar ] 8.[ncbi.nlm.nih.gov]

  • Heart Failure

    Health status in patients with chronic fatigue syndrome and in general population and disease comparison groups. Am J Med 1996 ; 101 : 281 –90.[doi.org] The actuarial survival rates of persons who are homozygous for the mutation of the hemochromatosis gene C282Y have been reported to be 95%, 93%, and 66%, at 5, 10, and 20[doi.org] Types of participants Adult participants with chronic heart failure, defined as a clinical syndrome characterised by breathlessness and fatigue that is caused by an inability[doi.org]

  • Liver Cirrhosis

    fatigue syndrome 3324·6 (1600·3 to 7347·9) 143·7 ( 0·3 to 564·7) 119·8 ( 10·1 to 498·7) 682·0 (295·2–1 608·9) 140·8 ( 0·2 to 558·0) 117·6 ( 9·8 to 494·1) Yellow fever 2·8[ncbi.nlm.nih.gov] We herein report the assessment of glycemic control in a 41-year-old man with dehydrated hereditary stomatocytosis and a PIEZO1 gene mutation complicated by diabetes mellitus[ncbi.nlm.nih.gov] Dengue episodes aggregate 1409·2 (937·6 to 2943·8) 134·1 ( 3·8 to 521·2) 110·8 ( 13·2 to 459·0) 82·1 (45·0–183·9) 141·4 (0·4 to 549·2) * 117·9 ( 9·4 to 486·7) Post-dengue chronic[ncbi.nlm.nih.gov]

  • Cryptogenic Cirrhosis

    Because of the discovery of the candidate gene (HFE) for hereditary hemochromatosis, we may now be able to screen high-risk patient populations for the abnormal mutation ([ncbi.nlm.nih.gov] Confusion, lethargy Hepatic encephalopathy Dyspnea, hypoxia Hepatopulmonary syndrome Portopulmonary hypertension Fatigue, pallor Anemia due to bleeding, hypersplenism, undernutrition[merckmanuals.com] […] with deficiency of folate (or iron or vitamin B 12 ), chronic disease, or effects of alcohol (eg, bone marrow suppression) Fluid overload, oliguria, symptoms of renal failure[merckmanuals.com]

  • Constitutional Anemia due to Iron Metabolism Disorder

    Red clover can be useful in the long-term treatment of auto-immune conditions such as rheumatoid arthritis and chronic fatigue syndrome.[herbaleducation.net] Hereditary hemochromatosis : Aetna considers genetic testing for HFE gene mutations medically necessary for persons who meet all of the following criteria: Member who has[aetna.com] It is known as an “alterative,” a substance that alters chronic conditions.[herbaleducation.net]

  • Hereditary Hyperekplexia

    Syndrome chronic atrial and intestinal dysrhythmia chronic fatigue syndrome Chronobiology Disorders Chudley-Mccullough syndrome Chudley-Rozdilsky Syndrome Churg-Strauss syndrome[rgd.mcw.edu] […] type 1 (C282Y and H63D mutation; complete HFE gene analysis on request) Sequencing of hotspots Sequencing of all coding exons of the gene Deletion and duplication analysis[cegat.de] Chromosome 4q- Syndrome chromosome 5q deletion syndrome Chromosome 6 Ring Syndrome Chromosome 7 Ring Syndrome Chromosome Xp11.3 Deletion Syndrome Chromosome Xq Duplication[rgd.mcw.edu]

  • Optic Atrophy-Intellectual Disability Syndrome

    Symptoms include poor muscle tone, especially of the neck muscles, poor visual tracking or blindness, and severe intellectual disability (PubMedHealth2) Chronic Fatigue Syndrome[richardsonthebrain.com] HEREDITARY HEMOCHROMATOSIS (3 MUTATIONS) CPT CODE: 81256 HEREDITARY HEMOCHROMATOSIS (KNOWN MUTATION) CPT CODE: 81400 Go to top HUNTINGTON DISEASE GENE: HTT (huntingtin) CHROMOSOMAL[chginc.org] Hereditary hemochromatosis : Aetna considers genetic testing for HFE gene mutations medically necessary for persons who meet all of the following criteria: Member who has[aetna.com]

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