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Cardiomyopathy. Like Mother, Like Daughter? A New Phenotype for a MYH7 Mutation

dc.contributor.authorAbreu, S
dc.contributor.authorTrigo, C
dc.contributor.authorPinto, MF
dc.date.accessioned2024-05-09T14:57:22Z
dc.date.available2024-05-09T14:57:22Z
dc.date.issued2021
dc.description.abstractWe report the case of a six-year-old girl referred to our department due to her mother's diagnosis of hypertrophic cardiomyopathy. Initial evaluation revealed restrictive physiology on echocardiography and cardiac catheterization. Genetic analysis of both mother and daughter revealed the same genetic variant at the MYH7 gene. Notably, although the genetic mutation was the same, the phenotype differed, resulting in different management and prognosis. The daughter received a heart transplant at the age of 20 due to pulmonary hypertension's early development, whereas the mother was under heart failure medical therapy. This case relevance lies in this specific mutation, which to our knowledge, has not been previously associated with restrictive phenotype, but also on the importance of early referral of family members.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationProg Pediatr Cardiol. 2021;61:101348pt_PT
dc.identifier.doi10.1016/j.ppedcard.2021.101348pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4893
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.subjectHSM CAR PEDpt_PT
dc.subjectRestrictive Cardiomyopathypt_PT
dc.subjectHypertrophic Cardiomyopathypt_PT
dc.subjectPhenotypept_PT
dc.subjectMYH7 Mutationpt_PT
dc.titleCardiomyopathy. Like Mother, Like Daughter? A New Phenotype for a MYH7 Mutationpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.startPage101348pt_PT
oaire.citation.titleProgress in Pediatric Cardiologypt_PT
oaire.citation.volume61pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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