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Results 1 - 10 of 10 for Short QT syndrome 1
  1. Short QT syndrome 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov SHORT QT SYNDROME 1; SQT1 SHORT QT SYNDROME 2; SQT2 SHORT QT SYNDROME 3; SQT3 PubMed ...
    https://medlineplus.gov/genetics/condition/short-qt-syndrome - Genetics
  2. KCNJ2 gene 
    ... novel gain-of-function KCNJ2 mutation associated with short-QT syndrome impairs inward rectification of Kir2.1 currents. Cardiovasc Res. 2012 Mar 15;93(4): ...
    https://medlineplus.gov/genetics/gene/kcnj2 - 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. ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  4. KCNH2 gene 
    ... Brugada P, Antzelevitch C. Sudden death associated with short-QT syndrome linked to mutations in HERG. Circulation. 2004 Jan 6;109(1):30-5. doi: 10.1161/01.CIR.0000109482. ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  5. CACNA1C gene 
    ... in various tissues. MedlinePlus Genetics provides information about Short QT syndrome More About This Health Condition Variants (also known ... affected individuals have heart problems separate from long QT syndrome. The severity of ... dihydropyridine-sensitive, alpha-1 subunit calcium channel, L type, alpha 1 polypeptide, ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
  6. Andersen-Tawil syndrome 
    ... on PubMed Modell SM, Lehmann MH. The long QT syndrome family of cardiac ... aspects. Int J Cardiol. 2013 Dec 5;170(1):1-16. doi: 10.1016/j.ijcard.2013. ...
    https://medlineplus.gov/genetics/condition/andersen-tawil-syndrome - Genetics
  7. Weill-Marchesani syndrome 
    ... Weill-Marchesani syndrome Genetic Testing Registry: Weill-Marchesani syndrome 1 Weill-Marchesani syndrome National Organization for Rare Disorders (NORD) WEILL-MARCHESANI SYNDROME 1; WMS1 WEILL-MARCHESANI SYNDROME 2; WMS2 PubMed Cecchi ...
    https://medlineplus.gov/genetics/condition/weill-marchesani-syndrome - Genetics
  8. KCNQ1OT1 gene 
    ... KCNQ1-AS2 KCNQ10T1 KvDMR1 KvLQT1-AS LIT1 long QT intronic transcript 1 Tests of KCNQ1OT1 PubMed KCNQ1-OPPOSITE STRAND/ANTISENSE ... study of Beckwith-Wiedemann syndrome and Silver-Russell syndrome cases. Hum Mol Genet. 2012 Jan 1;21(1):10-25. doi: 10.1093/hmg/ ...
    https://medlineplus.gov/genetics/gene/kcnq1ot1 - Genetics
  9. Dilated cardiomyopathy with ataxia syndrome 
    ... blood efficiently. Some affected individuals also have long QT syndrome, which is a heart condition that causes the ... problems and movement difficulties, most individuals with DCMA syndrome grow ... stature. Additionally, many affected individuals have mild intellectual ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  10. 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