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Electrocardiographic features of children with Duchenne muscular dystrophy

20 Aug 2022

Abstract excerpt

Duchenne muscular dystrophy (DMD) is a clinically common X-linked recessive myopathy, which is caused by mutation of the gene encoding dystrophin on chromosome Xp21. The onset of heart injury in children with DMD is inconspicuous, and the prognosis is poor once it develops to the stage of heart failure. Cardiovascular complications remain an important cause of death in this patient population. At present,...

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PMID: 35987773
DOI: 10.1186/s13023-022-02473-9

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