28
Mar
Hello: This is a diagnosis! Your doctor for more than two integrated hospital for treatment! Visiting Beijing Fu Wai Hospital for diagnosis and treatment! The following knowledge, please make reference to: hypertrophic cardiomyopathy with left ventricular and (or ) is characterized by right ventricular hypertrophy, usually asymmetric septal hypertrophy and involvement. Some patients may be asymptomatic, and physical examination because of sudden death or discovery. The most common symptom is difficulty breathing. Angina, fatigue, syncope and syncope aura are also common. Children and adolescents, syncope, and syncope aura increased the risk of sudden death, it is recommended in patients with early treatment. Such patients may have a family history, the proposed screening of family members of patients. Chest X-ray examination: cardiac enlargement and more obvious. Ultrasound diagnosis of this disease is important, to show wall thickening of the heart and the presence or absence of outflow obstruction. Hypertrophic cardiomyopathy is a congenital or acquired it? Hypertrophic cardiomyopathy is familial polygenic disease, 50% of the patients showed autosomal dominant inheritance, 40% of spontaneous mutations. Spontaneous gene mutation, 50% chance of genetic disease can be caused by the next generation. Therefore, the use of echocardiography to screen family members of patients have significant value. A variety of hypertrophic cardiomyopathy genotype, clinical manifestations of

various genotypes (age, symptoms, prognosis) were quite different. HCM the most common symptoms? Most of hypertrophic cardiomyopathy without clinical symptoms, but in the known family screening of patients found that patients with clinical symptoms, the most common symptoms are: 1. Shortness of breath: 90% occurred in symptomatic patients with left ventricular diastolic function insufficiency due to left ventricular filling is limited, left atrial and pulmonary vein hypertension related. 2. Angina pectoris: appeared in 75% of symptomatic patients, and myocardial mass increased, decreased coronary reserve capacity expansion, ventricular end diastolic pressure elevation induced subendocardial myocardial ischemia and myocardial oxygen supply and demand like contradictions related. 3. Syncope and threatened syncope: cardiac output and decreased movement or arrhythmia related to increased risk of sudden death (children and adolescents may be the first symptom of sudden death.) Non-invasive laboratory tests are helpful in the diagnosis of hypertrophic cardiomyopathy? Valuable non-invasive laboratory tests, including: ECG, X ray, ultrasound cardiogram. ECG may show normal, but mostly symptomatic patients is not normal, nonspecific ST-T changes, left ventricular high voltage, of inferi
Asymmetric hypertrophic cardiomyopathy (no obstruction)? ? ? ? ? Asymmetry of hypertrophic obstructive cardiomyopathy without help! ! !
Illnesses: no asymmetry in hypertrophic obstructive cardiomyopathy
Q: disease description (main symptom onset): Hello Doctor, I am 24 years old with congenital hypertrophic cardiomyopathy asymmetry before the age of 23 tired climbing stairs in addition to the other related to .
Hubei Provincial People's Hospital, Department of Cardiology, Hong Jiang Reply:
If convenient, you can come to my hospital outpatient treatment. Jiang Hong details non-symmetric non-obstructive hypertrophic cardiomyopathy
Illnesses: non-symmetric non-obstructive hypertrophic cardiomyopathy
Q: disease description (time of onset, the main symptom, visiting hospitals, etc.): used to treat and effectiveness: How do want to help: What can surgery? About how much it costs?
Hubei Provincial People's Hospital, Cardiovascular Surgery, Wu Zhiyong replies:
Could cost 4 million Tel 18971490330 E-mail wuzhiyong2008@yeah.net Details asymmetric hypertrophic cardiomyopathy 10 years of pacemaker
Asymmetric hypertrophic obstructive cardiomyopathy, mitral regurgitationMale, 58 years old, hypertrophic obstructive cardiomyopathy to therapy
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