Search
Descriptor English: Wolff-Parkinson-White Syndrome
Descriptor Spanish: Síndrome de Wolff-Parkinson-White
Descriptor síndrome de Wolff-Parkinson-White
Entry term(s) síndrome WPW
Scope note: 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.
Descriptor Portuguese: Síndrome de Wolff-Parkinson-White
Descriptor French: Syndrome de Wolff-Parkinson-White
Entry term(s): Syndrome WPW
Syndrome de WPW
Tree number(s): C14.280.067.780.977
C14.280.123.750.977
C16.131.240.400.980
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D014927
Scope note: 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.
Allowable Qualifiers: BL sang
CF liquide cérébrospinal
CI induit chimiquement
CL classification
CO complications
DG imagerie diagnostique
DH diétothérapie
DI diagnostic
DT traitement médicamenteux
EC économie
EH ethnologie
EM embryologie
EN enzymologie
EP épidémiologie
ET étiologie
GE génétique
HI histoire
IM immunologie
ME métabolisme
MI microbiologie
MO mortalité
NU soins infirmiers
PA anatomopathologie
PC prévention et contrôle
PP physiopathologie
PS parasitologie
PX psychologie
RH rééducation et réadaptation
RT radiothérapie
SU chirurgie
TH thérapie
UR urine
VE médecine vétérinaire
VI virologie
DeCS ID: 15327
Unique ID: D014927
NLM Classification: WG 330.5.P7
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1966/01/01
Date of Entry: 1999/01/01
Revision Date: 2017/06/20
Syndrome de Wolff-Parkinson-White - Preferred
Concept UI M0022990
Preferred term Syndrome de Wolff-Parkinson-White
Entry term(s) Syndrome WPW
Syndrome de WPW



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.


Go to survey