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Article

Cardiac involvement in two rare neuromuscular diseases: LAMA2-related muscular dystrophy and SELENON-related myopathy.

Neuromuscular disorders : NMD - 1 Aug 2022

Bouman Karlijn, Gubbels Madelief, van den Heuvel Frederik M A, Groothuis Jan T, Erasmus Corrie E, Nijveldt Robin, Udink Ten Cate Floris E A, Voermans Nicol C

Abstract excerpt

LAMA2-related muscular dystrophy (LAMA2-MD) and SELENON(SEPN1)-related myopathy (SELENON-RM) are rare neuromuscular diseases caused by mutations in the LAMA2 and SELENON (SEPN1) gene, respectively. Systematic reviews on cardiac features in both neuromuscular diseases are lacking. This scoping review aims to elucidate the cardiac involvement in LAMA2-MD or SELENON-RM. Three electronic databases (PubMed, Embase and...

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PMID: 35868898
DOI: 10.1016/j.nmd.2022.06.004

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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