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1,030 Possible Causes for Mutation in the Hereditary Hemochromatosis Gene, Nocturnal Paroxysmal Dyspnea, T Wave Inversion

  • Cardiomyopathy

    ECG T-wave inversion in right precordial leads (V 2 and V 3 ) 2. SAECG Late potentials seen on signal-averaged ECG 3.[] Symptoms: Patients with cardiomyopathy will typically present with dyspnea, orthopnea, paroxysmal nocturnal dyspnea, bilateral edema, and fatigue.[] These symptoms of heart failure most commonly include dyspnea , orthopnea , paroxysmal nocturnal dyspnea , and fluid retention. How Is Postpartum Cardiomyopathy Treated?[]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Coronary Atherosclerosis

    […] or appearance or disappearance of localized ST-elevation followed by T-wave inversion in two or more standard electrocardiograph leads; (c) increase in concentration of serum[] The ECG can show ST segment shifts and/or T-wave inversions as signs of heart ischemia or injury. However, there are electrically silent areas in the standard monitors.[] […] electrocardiograph leads; (b) thrombolysis for suspected MI (as indicated by localized ST-elevation in two or more standard electrocardiograph leads) even without later development of T-wave[]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Aortic Valve Stenosis

    At this point there may be signs of ventricular strain pattern (ST segment depression and T wave inversion) on the EKG, suggesting subendocardial ischemia.[] Other symptoms associated with AS are related to cardiac failure, such as paroxysmal nocturnal dyspnea, orthopnea, and dyspnea on exertion.[] The patient also presented dyspnea on minimal exertion, orthopnea, paroxysmal nocturnal dyspnea and edema of lower limbs. The patient denied fever.[]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Dilated Cardiomyopathy

    Takotsubo cardiomyopathy is characterized by the basal hypercontractility and apical ballooning of the left ventriculum and T-wave inversion in the electrocardiogram.[] 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[] The main role of ECG is to detect evidence of myocardial ischemia (pathologic Q waves with ST elevation and T wave inversion in leads I, aVL, V 5, V 6 ) that might point to[]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Heart Failure

    inversion (the "cerebral T-wave").[] Major criteria: · Paroxysmal nocturnal dyspnea · Neck vein distention · Rales · Radiographic cardiomegaly (increasing heart size on chest radiography) · Acute pulmonary edema[] 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[]

  • Primary Cardiomyopathy

    […] with no history of CAD, and frequent T-wave inversion.[] Patients present with an abrupt onset of angina-like chest pain, and have diffuse T-wave inversion, sometimes preceded by ST-segment elevation, and mild cardiac enzyme elevation[] […] 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[]

    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[] nocturnal dyspnea) Chest pain or pressure may be present along with the above symptoms Fatigue and weakness are commonly associated with cardiomyopathy Dizziness and lightheadedness[] […] patients in whom the additional volume cannot be pumped out by the left ventricle, there is a significant reduction in vital capacity and pulmonary compliance with resultant dyspnea[]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Acute Myocarditis

    Abstract BACKGROUND: The pathophysiologic mechanisms and the prognostic meaning of electrocardiographic (ECG) T-wave inversion (TWI) occurring in a subgroup of patients with[] Thereafter, T-wave inversion typically ensues. The T-wave inversion may be discrete and lasts for one month.[] ST-abnormalities were defined as significant ST-segment elevation and/or significant ST-segment depression and/or T-wave inversion [ 7 ].[]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Secondary Cardiomyopathy

    These may include electrocardiogram (ECG) changes of QT prolongation and T wave inversion, elevated biochemical markers of myocardial damage and heart failure, and decreased[] nocturnal dyspnea, and edema.[] inversion in leads I and aVL ( 3mm) (with QRS–T wave axis difference 30 ), V3–V6 ( 3mm) or II and III and aVF ( 5mm) Abnormal Q ( 40 ms or 25% R wave) in at least two leads[]

    Missing: Mutation in the Hereditary Hemochromatosis Gene
  • Viral Myocarditis

    On arrival at the ED a repeat EKG shows some ST elevations in V4-V6, without any reciprocal changes or T wave inversions.[]

    Missing: Mutation in the Hereditary Hemochromatosis Gene

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