Autopsy of a patient with restrictive cardiomyopathy with and MYH7 mutation

• المؤلفون الرئيسيون: Hiroaki Kawano (مؤلف), Koichi Kawamura (مؤلف), Munetake Kanda (مؤلف), Nozomi Ueki (مؤلف), Muneo Tanigawa (مؤلف), Mitsuaki Ishijima (مؤلف), Yuji Matsumoto (مؤلف), Masahiro Nakashima (مؤلف), Koji Maemura (مؤلف)
• التنسيق: كتاب
• منشور في: Elsevier, 2021-11-01T00:00:00Z.
• الموضوعات: article
• الوصول للمادة أونلاين: Connect to this object online.

Restrictive cardiomyopathy (RCM) is a rare type of primary myocardial disease, and its pathological features remain unclear. We report the case of a 78-year-old Japanese woman with RCM and MHY7 mutation who died of heart failure 13 years after the diagnosis. Upon autopsy, focal myocyte amorphous deg...