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Descritor em português: Síndrome de Wolff-Parkinson-White
Descritor em inglês: Wolff-Parkinson-White Syndrome
Descritor em espanhol: Síndrome de Wolff-Parkinson-White
Descritor síndrome de Wolff-Parkinson-White
Termo(s) alternativo(s) síndrome WPW
Nota de escopo: Forma de pre-excitación ventricular caracterizada por un intervalo PR corto y un intervalo QRS largo con una onda delta. En este síndrome, el impulso auricular se conduce hasta los VENTRÍCULOS CARDIACOS a través de una vía accesoria localizada entre la pared de las aurículas derecha o izquierda y los ventrículos, conocida como fascículo de Kent. La forma hereditaria puede estar causada por una mutación en el gen PRKAG2 que codifica una subunidad reguladora gamma-2 de la proteína cinasa activada por AMP.
Descritor em francês: Syndrome de Wolff-Parkinson-White
Termo(s) alternativo(s): Anomalous Ventricular Excitation Syndrome
Auriculoventricular Accessory Pathway Syndrome
False Bundle-Branch Block Syndrome
Syndrome, WPW
Syndrome, Wolf-Parkinson-White
Syndrome, Wolff-Parkinson-White
Ventricular Pre-Excitation with Arrhythmia
WPW Syndrome
Wolf Parkinson White Syndrome
Wolf-Parkinson-White Syndrome
Wolff Parkinson White Syndrome
Código(s) hierárquico(s): C14.280.067.780.977
C14.280.123.750.977
C16.131.240.400.980
Identificador Único RDF: https://id.nlm.nih.gov/mesh/D014927
Nota de escopo: A form of ventricular pre-excitation characterized by a short PR interval and a long QRS interval with a delta wave. In this syndrome, atrial impulses are abnormally conducted to the HEART VENTRICLES via an ACCESSORY CONDUCTING PATHWAY that is located between the wall of the right or left atria and the ventricles, also known as a BUNDLE OF KENT. The inherited form can be caused by mutation of PRKAG2 gene encoding a gamma-2 regulatory subunit of AMP-activated protein kinase.
Qualificadores permitidos: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Identificador DeCS: 15327
ID do descritor: D014927
Classificação da NLM: WG 330.5.P7
Documentos indexados na Biblioteca Virtual em Saúde (BVS): Clique aqui para acessar os documentos da BVS
Data de estabelecimento: 01/01/1966
Data de entrada: 01/01/1999
Data de revisão: 20/06/2017
Wolff-Parkinson-White Syndrome - Conceito preferido
Identificador do conceito M0022990
Nota de escopo A form of ventricular pre-excitation characterized by a short PR interval and a long QRS interval with a delta wave. In this syndrome, atrial impulses are abnormally conducted to the HEART VENTRICLES via an ACCESSORY CONDUCTING PATHWAY that is located between the wall of the right or left atria and the ventricles, also known as a BUNDLE OF KENT. The inherited form can be caused by mutation of PRKAG2 gene encoding a gamma-2 regulatory subunit of AMP-activated protein kinase.
Termo preferido Wolff-Parkinson-White Syndrome
Termo(s) alternativo(s) Anomalous Ventricular Excitation Syndrome
Auriculoventricular Accessory Pathway Syndrome
False Bundle-Branch Block Syndrome
Syndrome, WPW
Syndrome, Wolf-Parkinson-White
Syndrome, Wolff-Parkinson-White
Ventricular Pre-Excitation with Arrhythmia
WPW Syndrome
Wolf Parkinson White Syndrome
Wolf-Parkinson-White Syndrome
Wolff Parkinson White Syndrome



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