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Updated: Jun 26, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
An infant with congenital nemaline myopathy and hypertrophic cardiomyopathy
Mizue Nakajima1, Yoshio Shima, Sakae Kumasaka
1Department of Pediatrics, Japanese Red Cross Katsushika Maternity Hospital, Tokyo, Japan. s4019@nms.ac.jp
Abstract:
We describe an infant with nemaline myopathy accompanied by hypertrophic cardiomyopathy. The patient required long-term, intermittent positive-pressure ventilation after birth owing to muscle weakness, and cardiac failure developed during infancy. We diagnosed hypertrophic cardiomyopathy with outflow tract obstruction, and treated the heart failure with beta-adrenergic and angiotensin II receptor blockers. We discuss the prognosis of nemaline myopathy combined with hypertrophic cardiomyopathy.
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