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Results 1 - 9 of 9 for Short QT syndrome 3
  1. Short QT syndrome 
    ... SYNDROME 1; SQT1 SHORT QT SYNDROME 2; SQT2 SHORT QT SYNDROME 3; SQT3 PubMed Bjerregaard P, Gussak I. Short QT ... 3(4):611-7. doi: 10.1586/14779072.3.4.611. Citation on PubMed
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
  2. KCNH2 gene 
    ... N588K in KCNH2: a link to arrhythmogenesis in short QT syndrome. Cardiovasc Res. 2005 Aug 15;67(3):498-509. doi: 10.1016/j.cardiores.2005. ... Wolpert C, Gaita F, Giustetto C, Borggrefe M. Short QT syndrome. Cardiovasc Res. 2005 Aug 15;67(3):357-66. doi: 10.1016/j.cardiores.2005. ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  3. KCNQ1 gene 
    ... novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero. Cardiovasc Res. 2005 Dec 1;68(3):433-40. doi: 10.1016/j.cardiores.2005. ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  4. KCNJ2 gene 
    ... gene can also cause a heart condition called short QT syndrome, which is a type of arrhythmia. In people ... the KCNJ2 gene have been found to cause short QT syndrome in a small number of affected families. These ...
    https://medlineplus.gov/genetics/gene/kcnj2 - Genetics
  5. Andersen-Tawil syndrome 
    ... on PubMed Modell SM, Lehmann MH. The long QT syndrome family of cardiac ion channelopathies: a HuGE review. Genet Med. 2006 Mar;8(3):143-55. doi: 10.1097/01.gim.0000204468. ...
    https://medlineplus.gov/genetics/condition/andersen-tawil-syndrome - Genetics
  6. Weill-Marchesani syndrome 
    ... Marchesani syndrome include short stature, eye abnormalities, unusually short ... this condition ranges from 4 feet, 3 inches to 5 feet, 2 inches.An eye ...
    https://medlineplus.gov/genetics/condition/weill-marchesani-syndrome - Genetics
  7. Dilated cardiomyopathy with ataxia syndrome 
    ... blood efficiently. Some affected individuals also have long QT syndrome, which is a heart condition that causes the ... have high urine levels of another acid called 3-methylglutaric acid. DCMA syndrome is a very rare disorder. Approximately 30 cases ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  8. Glycogen storage disease type 0 
    ... heart's normal rhythm (arrhythmia) known as long QT syndrome. In all affected individuals, muscle GSD 0 impairs ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  9. KCNQ1OT1 gene 
    ... doi: 10.4161/rna.7113. Epub 2008 Oct 3. Citation on PubMed Kanduri C. Kcnq1ot1: a chromatin ... Squire J. Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular ...
    https://medlineplus.gov/genetics/gene/kcnq1ot1 - Genetics