ArticleFrontiers in cardiovascular medicine2023
Case report: A rare case of left ventricular noncompaction in two Chinese siblings with becker muscular dystrophy caused by deletion of exons 10 to 12 in the
Article in Frontiers in cardiovascular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Becker muscular dystrophy (BMD) is an inherited X-linked recessive condition resulting from mutations of the Case report: In the present study, we identified a deletion mutation in exons 10 to 12 (EX10_12 del) of the Conclusion: This case further enriches our knowledge of the symptoms, genotype, cardiac performance, management, and prognosis of BMD patients complicated by LVNC. It is recommended that early comprehensive cardiac evaluation should be considered for patients with BMD to exclude LVNC, as this may have a significant impact on their prognosis.
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