Arq. Bras. Cardiol. 2023; 120(7): e20220560

Cardiac Rehabilitation in a Transplanted Person with Emery-Dreifuss Muscular Dystrophy

Maria Loureiro ORCID logo , Carlos Branco ORCID logo , João Duarte ORCID logo , Gonçalo Coutinho ORCID logo , Maria Manuela Martins ORCID logo , André Novo ORCID logo

DOI: 10.36660/abc.20220560

Abstract

Emery-Dreifuss muscular dystrophy is a rare hereditary neuromuscular disease. Its manifestations begin primarily in childhood. The most frequent manifestations are progressive muscle weakness, atrophy that usually begins in the scapula-vertebral region, extending later to the pelvic girdle, and spinal stiffness. Patients can also manifest cardiac involvement as palpitations, syncope, exercise intolerance, congestive heart failure, and variable heart rhythm disturbances. The presence and severity of these manifestations can vary according to the individual and the disease’s subtypes. Cardiac involvement is the most worrisome feature of this disease, and there are some reports of the need for heart transplantation in this dystrophy.

Cardiac Rehabilitation in a Transplanted Person with Emery-Dreifuss Muscular Dystrophy

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