Apical Hypertrophic Cardiomyopathy - Muthiah, Ramachandran
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Apical hypertrophic cardiomyopathy (apical HCM) is a rare variant of hypertrophic cardiomyopathy with a prevalence of 1-2 % in Asian population and carries a benign prognosis both in Asian and Japanese. It is usually silent in early stages and manifest in adults with a suspicion of typical ECG changes of giant T wave inversion in left precordial leads. Transthoracic echocardiography is the mainstay of non-invasive diagnosis and provide a heterogeneous appearance of it's morphological features with a spade shaped LV (left ventricular cavity). Background of this case study described the…mehr

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Produktbeschreibung
Apical hypertrophic cardiomyopathy (apical HCM) is a rare variant of hypertrophic cardiomyopathy with a prevalence of 1-2 % in Asian population and carries a benign prognosis both in Asian and Japanese. It is usually silent in early stages and manifest in adults with a suspicion of typical ECG changes of giant T wave inversion in left precordial leads. Transthoracic echocardiography is the mainstay of non-invasive diagnosis and provide a heterogeneous appearance of it's morphological features with a spade shaped LV (left ventricular cavity). Background of this case study described the echocardiographic manifestations of apical HCM in a 54 -year old asymptomatic male.
Autorenporträt
Dr. Ramachandran Muthiah, MBBS, MD, DM, FNB, ACCF.Presidente di tutte le nazioniMedico e cardiologo Morning Star Hospital, Marthandam, distretto di Kanyakumari, India.