cardiomyopathy, familial hypertrophic, type 9

A hereditary heart disorder (OMIM:613765) characterised by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum.
Clinical findings
Dyspnoea, syncope, collapse, palpitations, and chest pain triggered by exercise. The disorder has inter- and intrafamilial variability, ranging from benign and asymptomatic to malignant forms with high risk of cardiac failure and sudden cardiac death.
Molecular pathology
Caused by defects of TTN, which encodes a critical protein in striated muscle.

单词	cardiomyopathy, familial hypertrophic, type 9
释义	cardiomyopathy, familial hypertrophic, type 9 cardiomyopathy, familial hypertrophic, type 9 A hereditary heart disorder (OMIM:613765) characterised by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. Clinical findings Dyspnoea, syncope, collapse, palpitations, and chest pain triggered by exercise. The disorder has inter- and intrafamilial variability, ranging from benign and asymptomatic to malignant forms with high risk of cardiac failure and sudden cardiac death. Molecular pathology Caused by defects of TTN, which encodes a critical protein in striated muscle.
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