Literature DB >> 11466145

Familial Mahaim syndrome.

P Ott1, F I Marcus.   

Abstract

We describe the occurrence of Mahaim syndrome in a mother and her son. The occurrence of such a rare disorder in two members of a family is noteworthy, has not been reported before, and suggests the possibility of genetic transmission. A genetic transmission of supraventricular tachycardia has been described only in rare cases for the Wolff-Parkinson-White syndrome. No such data is available for the Mahaim syndrome.

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Year:  2001        PMID: 11466145      PMCID: PMC7027687          DOI: 10.1111/j.1542-474x.2001.tb00117.x

Source DB:  PubMed          Journal:  Ann Noninvasive Electrocardiol        ISSN: 1082-720X            Impact factor:   1.468


  7 in total

1.  Electrocardiographic findings in 122,043 individuals.

Authors:  R G HISS; L E LAMB
Journal:  Circulation       Date:  1962-06       Impact factor: 29.690

2.  Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Authors:  D C Wallace; G Singh; M T Lott; J A Hodge; T G Schurr; A M Lezza; L J Elsas; E K Nikoskelainen
Journal:  Science       Date:  1988-12-09       Impact factor: 47.728

Review 3.  The long QT syndromes: genetic basis and clinical implications.

Authors:  C E Chiang; D M Roden
Journal:  J Am Coll Cardiol       Date:  2000-07       Impact factor: 24.094

4.  Electrophysiologic abnormalities in patients with hypertrophic cardiomyopathy. A consecutive analysis in 155 patients.

Authors:  L Fananapazir; C M Tracy; M B Leon; J B Winkler; R O Cannon; R O Bonow; B J Maron; S E Epstein
Journal:  Circulation       Date:  1989-11       Impact factor: 29.690

5.  Radiofrequency catheter ablation of right atriofascicular (Mahaim) accessory pathways guided by accessory pathway activation potentials.

Authors:  J H McClelland; X Wang; K J Beckman; H A Hazlitt; M I Prior; H Nakagawa; R Lazzara; W M Jackman
Journal:  Circulation       Date:  1994-06       Impact factor: 29.690

6.  Familial occurrence of accessory atrioventricular pathways (preexcitation syndrome).

Authors:  H J Vidaillet; J C Pressley; E Henke; F E Harrell; L D German
Journal:  N Engl J Med       Date:  1987-07-09       Impact factor: 91.245

7.  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

  7 in total

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