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2,418 Possible Causes for Mutation in the Hereditary Hemochromatosis Gene, Nocturnal Paroxysmal Dyspnea, Ventricular Tachycardia

  • Cardiomyopathy

    Symptoms: Patients with cardiomyopathy will typically present with dyspnea, orthopnea, paroxysmal nocturnal dyspnea, bilateral edema, and fatigue.[symptoma.com] Most common mode of presentation was ventricular tachycardia (VT). Two patients had left ventricular (LV) systolic dysfunction.[ncbi.nlm.nih.gov] […] nonsustained ventricular tachycardia.[nejm.org]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Congestive Heart Failure

    Features due to left heart failure: Dyspnea, orthopnea and paroxysmal nocturnal dyspnea: These symptoms develop due to congestion of the lungs.[symptoma.com] With an increase in creatinine, he experienced 3 episodes of ventricular tachycardia and ventricular fibrillation.[ncbi.nlm.nih.gov] 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

    Major criteria: · Paroxysmal nocturnal dyspnea · Neck vein distention · Rales · Radiographic cardiomegaly (increasing heart size on chest radiography) · Acute pulmonary edema[web.archive.org] We describe the novel use of bilateral cardiac sympathectomy in a woman with end-stage heart failure caused by ventricular tachycardia refractory to standard medical therapy[ncbi.nlm.nih.gov] 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]

  • Pulmonary Edema

    […] or comorbid paroxysmal nocturnal dyspnea and orthopnea are present, even in patients with preeclampsia.[ncbi.nlm.nih.gov] Dysrhythmias New-onset rapid atrial fibrillation and ventricular tachycardia can be responsible for CPE.[emedicine.com] tachycardia, direct-current cardioversion For rapid atrial fibrillation, cardioversion is preferred.[merckmanuals.com]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Coronary Atherosclerosis

    研究成果 : ジャーナルへの寄稿 › 記事 Catheter ablation for verapamil-sensitive fascicular ventricular tachycardia guided by precise mapping using a multi-spline duodecapolar catheter with[kyushu-u.pure.elsevier.com] […] fibrillation; VT ventricular tachycardia.[onlinejacc.org] Fish oil supplementation and risk of ventricular tachycardia and ventricular fibrillation in patients with implantable defibrillators: a randomized controlled trial.[doi.org]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Dilated Cardiomyopathy

    The following are the symptoms with which a patient may present: fatigue, orthopnea, dyspnea on exertion, paroxysmal nocturnal dyspnea, increasing edema, weight gain, or an[symptoma.com] Here, we report a Chinese family with typical DCM, ventricular tachycardia, syncope, and SCD.[ncbi.nlm.nih.gov] At presentation she had dyspnea at rest, orthopnea and paroxysmal nocturnal dyspnea.[doi.org]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Ischemic Cardiomyopathy

    Pulmonary congestion reduces when the patient is in erect position, it results in improvement in symptoms. [1],[2],[5] Paroxysmal nocturnal dyspnea Paroxysmal nocturnal dyspnea[explainmedicine.com] BACKGROUND: Noninducibility of sustained monomorphic ventricular tachycardia (SMVT) postablation does not insure absence of later recurrence in patients with ischemic cardiomyopathy[ncbi.nlm.nih.gov] We report a patient with ischemic CMP, symptomatic PVCs, and monomorphic ventricular tachycardia (VT) despite attempts to control symptoms with two antiarrhythmic drugs.[ncbi.nlm.nih.gov]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Myocardial Fibrosis

    Additionally, fatigue, paroxysmal nocturnal dyspnea, and orthopnea may be present. Thromboembolic complications may occur in EMF.[emedicine.medscape.com] We present a case report of a 33-year old female patient with biventricular obstruction, extreme hypertrophy, septal myocardial fibrosis and episodes of ventricular tachycardia[ncbi.nlm.nih.gov] BACKGROUND: Hypertrophic cardiomyopathy (HCM) is associated with an increased risk of sudden cardiac death due to ventricular tachycardia (VT), and myocardial fibrosis reflects[ncbi.nlm.nih.gov]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Primary Cardiomyopathy

    nocturnal dyspnea, and edema.[aafp.org] […] catecholaminergic polymorphic ventricular tachycardia, short QT syndrome ) cardiomyopathies from mitochondrial myopathies mixed dilated cardiomyopathy restrictive cardiomyopathy[radiopaedia.org] […] atrial fibrillation (Paf)発作性心房細動 paroxysmal nocturnal dyspnea発作性夜間呼吸困難 paroxysmal supraventricular tachycardia(PSVT)発作性上室性頻拍 paroxysmal ventricular tachycardia (PVT)発作性心室頻拍[tokyo-med.ac.jp]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Acute Myocarditis

    We describe an unusual case of a 44-year-old woman who was hospitalized for ventricular tachycardia, deep asthenia and dyspnoea with no previous history of cardiac disease[ncbi.nlm.nih.gov] tachycardia.[ncbi.nlm.nih.gov] Sudden cardiovascular collapse due to ventricular fibrillation (VF), ventricular tachycardia (VT) and cardiac tamponade occurred.[ncbi.nlm.nih.gov]

    Missing: Mutation in the Hereditary Hemochromatosis Gene

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