2010
DOI: 10.1016/j.hrtlng.2009.10.012
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Clinical and genetic investigation of pediatric cases of Wolff-Parkinson-White syndrome in Tunisian families

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“…The preponderance of patients with the WPWS appear without definable causes, with far fewer affected individuals manifesting a familial variant. The mode of inheritance of WPWS (OMIM 194200) is autosomal dominant, attributed to a heterozygous mutation in the PRKAG2 gene from chromosome 7q36.1 that encodes for the 5′‐AMP‐activated protein kinase subunit gamma‐2 protein controlling cardiac intracellular energy 39,40 . Isolated instances of physical assault 41 or electrical injury 42 have resulted in the sudden onset of WPWS in previously unaffected individuals.…”
Section: Discussionmentioning
confidence: 99%
“…The preponderance of patients with the WPWS appear without definable causes, with far fewer affected individuals manifesting a familial variant. The mode of inheritance of WPWS (OMIM 194200) is autosomal dominant, attributed to a heterozygous mutation in the PRKAG2 gene from chromosome 7q36.1 that encodes for the 5′‐AMP‐activated protein kinase subunit gamma‐2 protein controlling cardiac intracellular energy 39,40 . Isolated instances of physical assault 41 or electrical injury 42 have resulted in the sudden onset of WPWS in previously unaffected individuals.…”
Section: Discussionmentioning
confidence: 99%