Literature DB >> 7069337

Familial Wolff-Parkinson-White syndrome.

B L Chia, F C Yew, S O Chay, A T Tan.   

Abstract

Familial occurrence of Wolff-Parkinson-White (WPW) syndrome is uncommon and to date only seven instances have been documented in the literature. We describe another unusual family in which the proband, his father and two of his five brothers (including one who died suddenly) showed WPW conduction. A younger sister showed evidence of Lown-Ganong-Levin (LGL) pre-excitation. This pedigree is consistent with autosomal dominant inheritance and supports the importance of testing asymptomatic family members of patients with WPW because it is a potentially life-threatening conduction disorder.

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Year:  1982        PMID: 7069337     DOI: 10.1016/s0022-0736(82)80016-2

Source DB:  PubMed          Journal:  J Electrocardiol        ISSN: 0022-0736            Impact factor:   1.438


  4 in total

1.  Intrauterine supraventricular tachycardia with a familial history of Lown-Ganong-Levine syndrome.

Authors:  G Bosi; P Guerrini; G P Garani; P Alboni
Journal:  Pediatr Cardiol       Date:  1986       Impact factor: 1.655

2.  20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.

Authors:  S R Lalani; J V Thakuria; G F Cox; X Wang; W Bi; M S Bray; C Shaw; S W Cheung; A C Chinault; B A Boggs; Z Ou; E K Brundage; J R Lupski; J Gentile; S Waisbren; A Pursley; L Ma; M Khajavi; G Zapata; R Friedman; J J Kim; J A Towbin; P Stankiewicz; S Schnittger; I Hansmann; T Ai; S Sood; X H Wehrens; J F Martin; J W Belmont; L Potocki
Journal:  J Med Genet       Date:  2008-09-23       Impact factor: 6.318

3.  Familial Hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3.

Authors:  C A MacRae; N Ghaisas; S Kass; S Donnelly; C T Basson; H C Watkins; R Anan; L H Thierfelder; K McGarry; E Rowland
Journal:  J Clin Invest       Date:  1995-09       Impact factor: 14.808

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

  4 in total

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