Literature DB >> 15741379

Association between fetal lymphedema and congenital cardiovascular defects in Turner syndrome.

Melissa L Loscalzo1, Phillip L Van, Vincent B Ho, Vladimir K Bakalov, Douglas R Rosing, Carol A Malone, Harry C Dietz, Carolyn A Bondy.   

Abstract

OBJECTIVES: Turner syndrome (TS) is associated with congenital cardiovascular defects (CCVDs), most commonly bicuspid aortic valve (BAV) and aortic coarctation (COARC), congenital renal anomalies, and fetal lymphedema. It has been theorized that compressive or obstructive effects of fetal lymphedema may actually cause cardiovascular and renal dysmorphogenesis in TS. The objective of this study was to determine whether there is a specific association between a history of fetal lymphedema and CCVDs in monosomy X, or TS, independent of karyotype or general severity of the phenotype.
METHODS: This was a prospective study of 134 girls and women who have TS (mean age: 30 years) and were clinically evaluated for evidence of fetal lymphedema, classified as central (signified by the presence of neck webbing) or peripheral (current or perinatal, or dysplastic fingernails). The presence of BAV and/or COARC was detected by magnetic resonance imaging combined with echocardiography, and renal anomalies were determined by ultrasound.
RESULTS: There is a strong association between developmental central lymphedema, signified by neck webbing, and the presence of BAV (chi2 = 10) and COARC (chi2 = 8). The association between webbed neck and CCVDs was independent of karyotype. There was, in contrast, no significant association between renal anomalies and webbed neck or CCVDs.
CONCLUSIONS: The strong, statistically significant association between neck webbing and the presence of BAV and COARC in TS suggests a pathogenetic connection between fetal lymphatic obstruction and defective aortic development. The presence of neck webbing in TS should alert the clinician to the possibility of congenital cardiovascular defects.

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Mesh:

Year:  2005        PMID: 15741379     DOI: 10.1542/peds.2004-1369

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  19 in total

1.  Collectrin gene screening in Turner syndrome patients with kidney malformation.

Authors:  L Pasquali; G d'Annunzio; R Gastaldi; E Di Battista; V Calcaterra; D Larizza; R Lorini; E D'Amato
Journal:  J Genet       Date:  2009-04       Impact factor: 1.166

2.  Altered lymphatics in an ovine model of congenital heart disease with increased pulmonary blood flow.

Authors:  Sanjeev A Datar; Eric G Johnson; Peter E Oishi; Michael Johengen; Eric Tang; Angela Aramburo; Jubilee Barton; Hsuan-Chang Kuo; Stephen Bennett; Konstantine Xoinis; Bhupinder Reel; Gokhan Kalkan; Eniko Sajti; Oscar Osorio; Gary W Raff; Michael A Matthay; Jeffrey R Fineman
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2011-12-29       Impact factor: 5.464

3.  Altered reactivity and nitric oxide signaling in the isolated thoracic duct from an ovine model of congenital heart disease with increased pulmonary blood flow.

Authors:  Sanjeev A Datar; Peter E Oishi; Wenhui Gong; Stephen H Bennett; Christine E Sun; Michael Johengen; Jun Maki; Rebecca C Johnson; Gary W Raff; Jeffrey R Fineman
Journal:  Am J Physiol Heart Circ Physiol       Date:  2014-02-14       Impact factor: 4.733

4.  The physical phenotype of girls and women with Turner syndrome is not X-imprinted.

Authors:  Carolyn A Bondy; Lea Ann Matura; Nicole Wooten; James Troendle; Andrew R Zinn; Vladimir K Bakalov
Journal:  Hum Genet       Date:  2007-01-23       Impact factor: 4.132

5.  Thyroid ultrasound in patients with Turner syndrome: influence of clinical and auxological parameters.

Authors:  V Calcaterra; C Klersy; T Muratori; C Caramagna; V Brizzi; R Albertini; D Larizza
Journal:  J Endocrinol Invest       Date:  2010-05-28       Impact factor: 4.256

6.  Disrupted NOS signaling in lymphatic endothelial cells exposed to chronically increased pulmonary lymph flow.

Authors:  Sanjeev A Datar; Wenhui Gong; Youping He; Michael Johengen; Rebecca J Kameny; Gary W Raff; Emin Maltepe; Peter E Oishi; Jeffrey R Fineman
Journal:  Am J Physiol Heart Circ Physiol       Date:  2016-05-13       Impact factor: 4.733

Review 7.  Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management.

Authors:  Angela E Lin; Craig T Basson; Elizabeth Goldmuntz; Pilar L Magoulas; Deborah A McDermott; Donna M McDonald-McGinn; Elspeth McPherson; Colleen A Morris; Jacqueline Noonan; Catherine Nowak; Mary Ella Pierpont; Reed E Pyeritz; Alan F Rope; Elaine Zackai; Barbara R Pober
Journal:  Genet Med       Date:  2008-07       Impact factor: 8.822

8.  Turner syndrome in childhood and adolescence.

Authors:  Kateri McCarthy; Carolyn A Bondy
Journal:  Expert Rev Endocrinol Metab       Date:  2008

9.  Horseshoe kidney malformation in Turner syndrome is not associated with HNF-1beta gene mutations.

Authors:  Elena D'Amato; Giuseppe d'Annunzio; Valeria Calcaterra; Vera Morsellino; Daniela Larizza; Renata Lorini
Journal:  Pediatr Nephrol       Date:  2007-10-06       Impact factor: 3.714

10.  KLF2-mediated disruption of PPAR-γ signaling in lymphatic endothelial cells exposed to chronically increased pulmonary lymph flow.

Authors:  Catherine J Morris; Rebecca J Kameny; Jason Boehme; Wenhui Gong; Youping He; Terry Zhu; Emin Maltepe; Gary W Raff; Jeffrey R Fineman; Sanjeev A Datar
Journal:  Am J Physiol Heart Circ Physiol       Date:  2018-04-06       Impact factor: 4.733

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