Midodrine hydrochloride and unexpected improvement in hypertrophic cardiomyopathy symptoms

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Management of symptoms in hypertrophic cardiomyopathy.

In 1957, Brock1 made the distinction between congenital subaortic stenosis characterized by a fibrous ridge and “functional subvalvar stenosis” resulting from “muscular hypertrophy,” describing 3 patients with the latter. Brock initially attributed the hypertrophy and resultant outflow obstruction to systemic hypertension, a conclusion he withdrew in a 1959 publication.2 Between these 2 publica...

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Hypertrophic Cardiomyopathy

Circulation Research is available at http://circres.ahajournals.org DOI: 10.1161/CIRCRESAHA.117.311059 Abstract: Hypertrophic cardiomyopathy (HCM) is a genetic disorder that is characterized by left ventricular hypertrophy unexplained by secondary causes and a nondilated left ventricle with preserved or increased ejection fraction. It is commonly asymmetrical with the most severe hypertrophy in...

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Hypertrophic cardiomyopathy (HCM) is an inherited cardiac disease with an incidence of about 1 in 500 individuals. It is characterized by asymmetrical hypertrophy of the left ventricle in the absence of other causes for hypertrophy. HCM can vary from essentially asymptomatic to highly malignant up to end-stage heart failure or cause life-threatening arrhythmias with sudden cardiac death particu...

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ژورنال

عنوان ژورنال: Archives of Cardiovascular Diseases

سال: 2016

ISSN: 1875-2136

DOI: 10.1016/j.acvd.2015.11.005