Literature DB >> 12695480

Williams syndrome associated with complete atrioventricular septal defect.

S Nakamoto1, T Saga, T Shinohara.   

Abstract

Williams syndrome is a genetic disorder associated with characteristic facies, supravalvar aortic stenosis, peripheral pulmonary stenosis, mental retardation, hypertension, premature aging of skin, and congenital cardiac defects. Many cardiac defects such as bicuspid aortic valve, mitral valve regurgitation, coarctation of the aorta, and ventricular or atrial septal defects are linked to the syndrome. Complete atrioventricular septal defect has rarely been associated with Williams syndrome and only one necropsy case has been reported in the literature. The long term follow up of Williams syndrome associated with complete atrioventricular septal defect is reported. During a 10 year follow up period, the pressure gradient in the ascending aorta did not increase despite narrowing of the ascending aorta as identified on an aortogram.

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Year:  2003        PMID: 12695480      PMCID: PMC1767652          DOI: 10.1136/heart.89.5.e15

Source DB:  PubMed          Journal:  Heart        ISSN: 1355-6037            Impact factor:   5.994


  10 in total

1.  The Williams elfin facies syndrome. A new perspective.

Authors:  K L Jones; D W Smith
Journal:  J Pediatr       Date:  1975-05       Impact factor: 4.406

2.  Supravalvular aortic stenosis.

Authors:  J C WILLIAMS; B G BARRATT-BOYES; J B LOWE
Journal:  Circulation       Date:  1961-12       Impact factor: 29.690

3.  Supravalvular aortic stenosis in association with mental retardation and a certain facial appearance.

Authors:  A J BEUREN; J APITZ; D HARMJANZ
Journal:  Circulation       Date:  1962-12       Impact factor: 29.690

4.  Specific impairment of cardiogenesis in mouse ES cells containing a human chromosome 21.

Authors:  T Inoue; T Shinohara; S Takehara; J Inoue; H Kamino; H Kugoh; M Oshimura
Journal:  Biochem Biophys Res Commun       Date:  2000-06-24       Impact factor: 3.575

5.  [Case of supravalvular aortic stenosis syndrome associated with complete endocardial cushion defect].

Authors:  S Hanya; M Natsuaki; T Morikawa; K Tatsuno; Y Imai
Journal:  Kyobu Geka       Date:  1974-06

6.  Mitral insufficiency in association with the syndrome of idiopathic hypercalcema of infancy.

Authors:  A M Vazquez; J R Zuberbuhler; F M Kenny
Journal:  J Pediatr       Date:  1968-12       Impact factor: 4.406

7.  Mitral valvular abnormalities associated with supravalvular aortic stenosis. Observations in 3 cases.

Authors:  A E Becker; M J Becker; J E Edwards
Journal:  Am J Cardiol       Date:  1972-01       Impact factor: 2.778

8.  Down syndrome phenotypes: the consequences of chromosomal imbalance.

Authors:  J R Korenberg; X N Chen; R Schipper; Z Sun; R Gonsky; S Gerwehr; N Carpenter; C Daumer; P Dignan; C Disteche
Journal:  Proc Natl Acad Sci U S A       Date:  1994-05-24       Impact factor: 11.205

9.  A new and rare form of Williams' syndrome.

Authors:  A Akçoral; D Ozaksoy; B Oran; N Narin; N T Cevik
Journal:  Acta Paediatr Jpn       Date:  1993-06

10.  Down syndrome: molecular mapping of the congenital heart disease and duodenal stenosis.

Authors:  J R Korenberg; C Bradley; C M Disteche
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

  10 in total
  5 in total

1.  Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions.

Authors:  Erfan Aref-Eshghi; Eric G Bend; Samantha Colaiacovo; Michelle Caudle; Rana Chakrabarti; Melanie Napier; Lauren Brick; Lauren Brady; Deanna Alexis Carere; Michael A Levy; Jennifer Kerkhof; Alan Stuart; Maha Saleh; Arthur L Beaudet; Chumei Li; Maryia Kozenko; Natalya Karp; Chitra Prasad; Victoria Mok Siu; Mark A Tarnopolsky; Peter J Ainsworth; Hanxin Lin; David I Rodenhiser; Ian D Krantz; Matthew A Deardorff; Charles E Schwartz; Bekim Sadikovic
Journal:  Am J Hum Genet       Date:  2019-03-28       Impact factor: 11.025

Review 2.  Copy number variants at Williams-Beuren syndrome 7q11.23 region.

Authors:  Giuseppe Merla; Nicola Brunetti-Pierri; Lucia Micale; Carmela Fusco
Journal:  Hum Genet       Date:  2010-05-01       Impact factor: 4.132

3.  Sudden unexpected death in a toddler with Williams syndrome.

Authors:  Henry F Krous; Carter Wahl; Amy E Chadwick
Journal:  Forensic Sci Med Pathol       Date:  2008-04-04       Impact factor: 2.007

Review 4.  Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome.

Authors:  Barbara R Pober; Mark Johnson; Zsolt Urban
Journal:  J Clin Invest       Date:  2008-05       Impact factor: 14.808

5.  Minoxidil versus placebo in the treatment of arterial wall hypertrophy in children with Williams Beuren Syndrome: a randomized controlled trial.

Authors:  Behrouz Kassai; Philippe Bouyé; Brigitte Gilbert-Dussardier; François Godart; Jean-Benoit Thambo; Massimiliano Rossi; Pierre Cochat; Pierre Chirossel; Stephane Luong; André Serusclat; Isabelle Canterino; Catherine Mercier; Muriel Rabilloud; Christine Pivot; Fabrice Pirot; Tiphanie Ginhoux; Stéphanie Coopman; Guillaume Grenet; François Gueyffier; Sylvie Di-Fillippo; Aurélia Bertholet-Thomas
Journal:  BMC Pediatr       Date:  2019-05-28       Impact factor: 2.125

  5 in total

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