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Updated: Aug 18, 2026

Single Myofiber Isolation and Culture from a Murine Model of Emery-Dreifuss Muscular Dystrophy in Early Post-Natal Development
Published on: July 1, 2020
A family of Emery-Dreifuss muscular dystrophy with extreme difference in severity
Yoshihisa Higuchi1, Masako Hongou, Kyoko Ozawa
1Department of Pediatrics, Utano National Hospital, Kyoto, Japan.
Abstract:
This report describes two patients, a father and son, with autosomal dominant Emery-Dreifuss muscular dystrophy. Although the father had the common phenotype, the son had a severe phenotype including early onset of weakness and fatal cardiomyopathy in childhood. Among the patients with severe phenotype of autosomal dominant Emery-Dreifuss muscular dystrophy, he is the first to have familial onset, and in the severe end of this disease spectrum.
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