Literature DB >> 16302915

Is Wolff-Parkinson-White syndrome a genetic disease?

Javed Ehtisham1, Hugh Watkins.   

Abstract

Family studies, and more recent molecular genetic investigations, indicate that the Wolff-Parkinson-White (WPW) syndrome and associated preexcitation disorders can have a substantial genetic component. Because preexcitation disorders are sometimes inherited as single gene disorders, key mechanistic insights can be gained that are expected to be relevant also to the more common multifactorial forms of these traits. Potentially, such insights will inform the future management of these conditions. Where WPW is inherited as a familial trait, with or without associated cardiac defects or a systemic syndrome, there are clinical genetic ramifications that are already of practical importance.

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Year:  2005        PMID: 16302915     DOI: 10.1111/j.1540-8167.2005.50139.x

Source DB:  PubMed          Journal:  J Cardiovasc Electrophysiol        ISSN: 1045-3873


  7 in total

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Review 2.  Abnormal ECG Findings in Athletes: Clinical Evaluation and Considerations.

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Journal:  Curr Treat Options Cardiovasc Med       Date:  2019-12-21

3.  Electrocardiographic features of Korean carbon disulfide poisoned subjects after discontinuation of exposure.

Authors:  Hyung-Joon Jhun; Sung-Il Cho; Mi-Jung Kim; Jidong Sung
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4.  Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.

Authors:  Zeynep H Coban-Akdemir; Wu-Lin Charng; Mahshid Azamian; Ingrid S Paine; Jaya Punetha; Christopher M Grochowski; Tomasz Gambin; Santiago O Valdes; Bryan Cannon; Gladys Zapata; Patricia P Hernandez; Shalini Jhangiani; Harsha Doddapaneni; Jianhong Hu; Fatima Boricha; Donna M Muzny; Eric Boerwinkle; Yaping Yang; Richard A Gibbs; Jennifer E Posey; Xander H T Wehrens; John W Belmont; Jeffrey J Kim; Christina Y Miyake; James R Lupski; Seema R Lalani
Journal:  Am J Med Genet A       Date:  2020-03-31       Impact factor: 2.802

5.  PRKAG2 mutation: An easily missed cardiac specific non-lysosomal glycogenosis.

Authors:  Varun Aggarwal; Nancy Dobrolet; Steven Fishberger; Jenny Zablah; Parul Jayakar; Zineb Ammous
Journal:  Ann Pediatr Cardiol       Date:  2015 May-Aug

6.  Expanding the phenotype of CACNA1C mutation disorders.

Authors:  Lindsey Gakenheimer-Smith; Lindsay Meyers; Derek Lundahl; Shaji C Menon; T Jared Bunch; Briana L Sawyer; Martin Tristani-Firouzi; Susan P Etheridge
Journal:  Mol Genet Genomic Med       Date:  2021-04-01       Impact factor: 2.183

7.  Isolated Wolff-Parkinson-White syndrome in identical twins.

Authors:  Michael E Field; Jennifer J Laffin; Jonathan J Langberg; Nicholas H Von Bergen
Journal:  HeartRhythm Case Rep       Date:  2018-02-09
  7 in total

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