Congenital Long QT Syndrome, Coinciding With Cavitary

MAC infection Mycobacterium avium complex QT prolongation cardiac arrest congenital long QT syndrome torsades de pointes

Journal

JACC. Case reports
ISSN: 2666-0849
Titre abrégé: JACC Case Rep
Pays: Netherlands
ID NLM: 101757292

Informations de publication

Date de publication:
01 Nov 2023
Historique:
received: 25 07 2023
revised: 28 08 2023
accepted: 07 09 2023
medline: 14 12 2023
pubmed: 14 12 2023
entrez: 14 12 2023
Statut: epublish

Résumé

Congenital long QT syndrome is a cardiac disorder leading to arrhythmias and sudden cardiac death. We present a case of a 55-year-old woman with altered mental status experiencing cardiac arrest caused by congenital long QT syndrome, coincidentally found with

Identifiants

DOI: 10.1016/j.jaccas.2023.102032 PMID: 38094215 PMC: PMC10715927
pubmed: 38094215
doi: 10.1016/j.jaccas.2023.102032
pii: S2666-0849(23)00366-2
pmc: PMC10715927
doi:

Types de publication

Case Reports

Langues

eng

Pagination

102032

Informations de copyright

© 2023 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.

Auteurs

Muhammad Ghallab (M)

Icahn School of Medicine at Mount Sinai, Queens Hospital Center, Internal Medicine Department, Queens, New York, USA.

Nazaakat Ahmed (N)

Icahn School of Medicine at Mount Sinai, Queens Hospital Center, Internal Medicine Department, Queens, New York, USA.

Zakaria Alagha (Z)

Department of Medicine, Marshall University Joan C. Edwards School of Medicine, Huntington, West Virginia, USA.

Daniel Miller (D)

Icahn School of Medicine at Mount Sinai, Queens Hospital Center, Internal Medicine Department, Queens, New York, USA.

Nso Nso (N)

Cardiology Department, University of Chicago, Northshore, Evanston, Illinois, USA.

Most Sirajum Munira (MS)

Icahn School of Medicine at Mount Sinai, Queens Hospital Center, Cardiology Department, Queens, New York, USA.

Classifications MeSH