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Concept information

Cardiovascular Diseases > Heart Diseases > Heart Defects, Congenital > Long QT Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Cardiovascular Abnormalities > Heart Defects, Congenital > Long QT Syndrome
Cardiovascular Diseases > Cardiovascular Abnormalities > Heart Defects, Congenital > Long QT Syndrome
Cardiovascular Diseases > Heart Diseases > Arrhythmias, Cardiac > Long QT Syndrome
Pathological Conditions, Signs and Symptoms > Pathologic Processes > Arrhythmias, Cardiac > Long QT Syndrome
Cardiovascular Diseases > Heart Diseases > Cardiac Conduction System Disease > Long QT Syndrome

Terme préférentiel

Long QT Syndrome  

Type

  • mesh:Descriptor

Définition

  • A condition that is characterized by episodes of fainting (SYNCOPE) and varying degree of ventricular arrhythmia as indicated by the prolonged QT interval. The inherited forms are caused by mutation of genes encoding cardiac ion channel proteins. The two major forms are ROMANO-WARD SYNDROME and JERVELL-LANGE NIELSEN SYNDROME.

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URI

http://data.loterre.fr/ark:/67375/JVR-X3F7D95G-2

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RDF/XML TURTLE JSON-LD Date de création 11/03/1985, dernière modification le 17/06/2019