Familial Hypertrophic Cardiomyopathy With Fasciculoventricular Accessory Pathway.
CMR, cardiac magnetic resonance
Danon disease
ECG, electrocardiogram
FVBT, fasciculoventricular bypass tract
HCM, hypertrophic cardiomyopathy
ICD, implantable cardioverter-defibrillator
LAMP-2, lysosome-associated membrane protein 2
MYBPC3, cardiac myosin binding protein C3
NSVT, nonsustained ventricular tachycardia
WPW, Wolff-Parkinson-White syndrome
accessory pathway
familial
hypertrophic cardiomyopathy
Journal
JACC. Case reports
ISSN: 2666-0849
Titre abrégé: JACC Case Rep
Pays: Netherlands
ID NLM: 101757292
Informations de publication
Date de publication:
16 Feb 2022
16 Feb 2022
Historique:
received:
20
04
2021
revised:
12
11
2021
accepted:
09
12
2021
entrez:
24
2
2022
pubmed:
25
2
2022
medline:
25
2
2022
Statut:
epublish
Résumé
Hypertrophic cardiomyopathy (HCM) is a common but an underdiagnosed condition. Fasciculoventricular bypass tract (FVBT) is rare. Concomitant presence of both conditions is well described in Danon disease. We report a case of familial HCM with FVBT linked to a heterozygous pathogenic variant, c.655G>C (p.Val219Leu), in the cardiac myosin binding protein C3 (MYBPC3) gene. (
Identifiants
pubmed: 35199016
doi: 10.1016/j.jaccas.2021.12.011
pii: S2666-0849(21)01087-1
pmc: PMC8855128
doi:
Types de publication
Case Reports
Langues
eng
Pagination
198-204Informations de copyright
© 2022 The Authors.
Déclaration de conflit d'intérêts
The authors have reported that they have no relationships relevant to the contents of this paper to disclose.
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