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Case report
Complex phenotype linked to a mutation in exon 11 of the lamin A/C gene: Hypertrophic cardiomyopathy, atrioventricular block, severe dyslipidemia and diabetes
Fenótipo complexo associado a uma mutação no exão 11 do gene da lâmina A/C: miocardiopatia hipertrófica, bloqueio auriculoventricular, dislipidemia grave e diabetes mellitus
Ana Rita G. Francisco
Corresponding author
ana.r.francisco@gmail.com

Corresponding author.
, Inês Santos Gonçalves, Fátima Veiga, Mónica Mendes Pedro, Fausto J. Pinto, Dulce Brito
Cardiology Department, Santa Maria University Hospital, CHLN, CAML, CCUL, Faculty of Medicine, University of Lisbon, Lisbon, Portugal
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ISSN: 08702551
Original language: English
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2025 11 88 32 120
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2025 3 58 26 84
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2023 11 33 35 68
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2020 2 45 21 66
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2017 12 47 24 71
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Revista Portuguesa de Cardiologia (English edition)
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