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Results 1 - 10 of 15 for Short QT syndrome type 2
  1. ... Short QT syndrome type 1 Genetic Testing Registry: Short QT syndrome type 2 Genetic Testing Registry: Short QT syndrome type 3 National Organization for Rare Disorders (NORD) ClinicalTrials. ...
  2. ... gene can also cause a heart condition called short QT syndrome, which is a ... or sudden death.At least two mutations in the KCNJ2 gene have been found ...
  3. ... Wolpert C, Gaita F, Giustetto C, Borggrefe M. Short QT syndrome. Cardiovasc Res. ... pathogenesis of long QT syndrome type 2. J Arrhythm. 2016 Oct;32(5):373-380. ...
  4. ... subunit voltage-gated calcium channel alpha subunit Cav1.2 Tests of CACNA1C PubMed CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-1C SUBUNIT; CACNA1C LONG QT SYNDROME 8; LQT8 NCBI Gene ClinVar Bozarth X, Dines ...
  5. ... cenobamate.tell your doctor if you have familial short QT syndrome (an inherited condition that causes irregular heartbeat, dizziness, ...
  6. ... in your family has or has ever had short QT syndrome (condition that increases the risk of irregular heartbeat, ...
  7. ... KCNJ2 gene mutations, the cause of Andersen-Tawil syndrome is usually unknown. These cases are classified as type 2 (ATS2). Studies suggest that variations in at least ...
  8. ... your family has or has ever had long QT syndrome (condition that increases the risk of developing an irregular heartbeat that may cause fainting or sudden death), or another type of irregular heart beat or heart rhythm problem, ...
  9. ... have no heart problems at all.By age 2, children with DCMA syndrome have ... stature. Additionally, many affected individuals have mild intellectual ...
  10. ... heart's normal rhythm (arrhythmia) known as long QT syndrome. In all affected individuals, muscle GSD 0 impairs ... MA. A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0. BMC Med Genet. 2010 Jan 5;11: ...
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