Nova mutação no gene PRKAG2 associado a parada cardiorrespiratória, insuficiência cardíaca congestiva e múltiplas vias acessórias / A novel mutation in the PRKAG2 gene associated with cardiorespiratory arrest, congestive heart failure and accessory pathways
RELAMPA, Rev. Lat.-Am. Marcapasso Arritm
;
27(3): 136-139, jul.-set. 2014.
Article
in Portuguese
| LILACS
| ID: lil-736744
RESUMO
Relata-se o caso de paciente do sexo masculino portador de síndrome de Wolff-Parkinson-White,hipertrofia ventricular e doença do sistema de condução, que apresentou duas paradas cardiorrespiratórias,insuficiência cardíaca congestiva e uma nova variação no gene PRKAG2.
ABSTRACT
We report the case of a male patient suffering from Wolff-Parkinson-White syndrome, ventricularhypertrophy, cardiac conduction system disease, who presented two cardiorespiratory arrests, congestive heartfailure and a new variation in the PRKAG2 gene.
Full text:
Available
Index:
LILACS (Americas)
Main subject:
Wolff-Parkinson-White Syndrome
/
Heart Arrest
Type of study:
Risk factors
Limits:
Adolescent
/
Humans
/
Male
Language:
Portuguese
Journal:
RELAMPA, Rev. Lat.-Am. Marcapasso Arritm
Journal subject:
Cardiology
Year:
2014
Type:
Article
Affiliation country:
Brazil
/
Spain
Institution/Affiliation country:
Escola Bahiana de Medicina e Saúde Pública/BR
/
Institut d'Investigació Biomèdica de Girona/ES
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