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52 Possible Causes for Mutation in the Hereditary Hemochromatosis Gene, Pericardial Effusion

  • Congestive Heart Failure

    effusion)[emedicine.medscape.com] 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] (in CHF or pneumonia), discrete loss of vascular markings (in pneumothorax), water-bottle heart (in pericardial effusion), and hyperinflation (in chronic obstructive pulmonary[clinicaladvisor.com]

  • Restrictive Cardiomyopathy

    We describe the evolution during pregnancy of a case of restrictive cardiomyopathy which first presented at 22 weeks' gestation with a large pericardial effusion.[ncbi.nlm.nih.gov] Cardiac Hemochromatosis Hereditary hemochromatosis (HH) is caused by increased absorption of dietary iron, which accumulates in various organs, leading to their dysfunction[circres.ahajournals.org] The left and right atrium may be markedly enlarged and a pericardial effusion may be present.[healio.com]

  • Heart Failure

    effusion)[emedicine.medscape.com] 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] Heart failure was evident on chest X-ray and 2D-echocardiogram showed global left ventricular hypokinesia with 40% ejection fraction and a thin layer of pericardial effusion[ncbi.nlm.nih.gov]

  • Thalassemia Minor

    The main clinical features are generalized edema and pleural and pericardial effusions as a result of congestive heart failure induced by severe anemia.[ncbi.nlm.nih.gov] […] of the hereditary hemochromatosis gene (HFE gene), iron overload may ensue.[ncbi.nlm.nih.gov] Hb Bart syndrome, the more severe form, is characterized by fetal onset of generalized edema, pleural and pericardial effusions, and severe hypochromic anemia, in the absence[ncbi.nlm.nih.gov]

  • Congenital Absence of Ductus Arteriosus

    effusion 1 8 Aneurysm ductus with thrombus 1 8 Hydrops foetalis 1 8 Microcystic lung changes 1 8 Five cases are described in more depth as an example of the findings.[academic.oup.com] Mutations of this gene are known to be associated with hereditary juvenile hemochromatosis ( 17, 18 ).[spandidos-publications.com] Pericardial effusion should be absent, or less than 2–4 mm.[intechopen.com]

  • Behçet Disease

    effusion.[dx.doi.org] 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] Pericarditis is common, variably manifesting as recurrent, hemorrhagic, or small asymptomatic pericardial effusion.[ped-rheum.biomedcentral.com]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    Other symptoms include elevated liver function, seizures, fluid around the heart (pericardial effusion), and blood clotting disorders.[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] 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]

  • Massive Hepatic Necrosis

    He did well until the 6th postoperative day, when he de- veloped evidence of pericardial effusion with cardiac tamponade.[nap.edu] Metabolic Disorders Hemochromatosis Hereditary hemochromatosis Mutations involving hereditary hemochromatosis gene HFE Unrestricted re-absorption of iron in the small intestines[slideshare.net] The chest film showed cardiac enlargement, suggestive of pericardial effusion. She had four operations under general anesthesia.[nap.edu]

  • Optic Atrophy-Intellectual Disability Syndrome

    Other symptoms include elevated liver function, seizures, fluid around the heart (pericardial effusion), and blood clotting disorders.[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] 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]

  • Familial Congenital Nasolacrimal Duct Obstruction

    Effusion Pericarditis Pericarditis, Constrictive Pericarditis, Tuberculous Pericoronitis Perimeningeal Infections Perinephritis Periodontal Abscess Periodontal Attachment[medgene.med.harvard.edu] 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] Peptic Ulcer Hemorrhage Peptic Ulcer Perforation Perceptual Disorders Periapical Abscess Periapical Diseases Periapical Granuloma Periapical Periodontitis Periarthritis Pericardial[medgene.med.harvard.edu]

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