Literature DB >> 18580689

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

Angela E Lin1, 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.   

Abstract

Cardiovascular abnormalities, especially structural congenital heart defects, commonly occur in malformation syndromes and genetic disorders. Individuals with syndromes comprise a significant proportion of those affected with selected congenital heart defects such as complete atrioventricular canal, interrupted arch type B, supravalvar aortic stenosis, and pulmonary stenosis. As these individuals age, they contribute to the growing population of adults with special health care needs. Although most will require longterm cardiology follow-up, primary care providers, geneticists, and other specialists should be aware of (1) the type and frequency of cardiovascular abnormalities, (2) the range of clinical outcomes, and (3) guidelines for prospective management and treatment of potential complications. This article reviews fundamental genetic, cardiac, medical, and reproductive issues associated with common genetic syndromes that are frequently associated with a cardiovascular abnormality. New data are also provided about the cardiac status of adults with a 22q11.2 deletion and with Down syndrome.

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Year:  2008        PMID: 18580689      PMCID: PMC2671242          DOI: 10.1097/gim.0b013e3181772111

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  253 in total

1.  Influence of chromosome 22q11.2 microdeletion on surgical outcome after treatment of tetralogy of fallot with pulmonary atresia.

Authors:  Adriano Carotti; Bruno Marino; Roberto M Di Donato
Journal:  J Thorac Cardiovasc Surg       Date:  2003-11       Impact factor: 5.209

2.  Multiple left-sided cardiac lesions in one of Noonan's original patients.

Authors:  J S Danetz; M T Donofrio; R P Embrey
Journal:  Cardiol Young       Date:  1999-11       Impact factor: 1.093

3.  A comparison of echocardiography and magnetic resonance imaging in cardiovascular screening of adults with Turner syndrome.

Authors:  Julia E Ostberg; Jocelyn A S Brookes; Carolyn McCarthy; Julian Halcox; Gerard S Conway
Journal:  J Clin Endocrinol Metab       Date:  2004-12       Impact factor: 5.958

4.  Prenatal sonographic diagnosis of Holt-Oram syndrome.

Authors:  T Tongsong; P Chanprapaph
Journal:  J Clin Ultrasound       Date:  2000-02       Impact factor: 0.910

5.  Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal.

Authors:  B Marino; M C Digilio; A Toscano; A Giannotti; B Dallapiccola
Journal:  J Pediatr       Date:  1999-12       Impact factor: 4.406

6.  Fetal aortic root dilation: a prenatal feature of the Loeys-Dietz syndrome.

Authors:  Valeria Viassolo; Mario Lituania; Maurizio Marasini; Harry Dietz; Fabrizio Benelli; Francesca Forzano; Francesca Faravelli
Journal:  Prenat Diagn       Date:  2006-11       Impact factor: 3.050

7.  Rapidly progressive obstructive cardiomyopathy in infants with Noonan's syndrome. Report of two cases.

Authors:  H D Hirsch; H Gelband; O Garcia; S Gottlieb; D M Tamer
Journal:  Circulation       Date:  1975-12       Impact factor: 29.690

Review 8.  Partial anomalous pulmonary vein connection: an underestimated cardiovascular defect in Ullrich-Turner syndrome.

Authors:  Susanne M Bechtold; Robert Dalla Pozza; Axel Becker; Anette Meidert; Christoph Döhlemann; Hans Peter Schwarz
Journal:  Eur J Pediatr       Date:  2004-01-10       Impact factor: 3.183

9.  Prevalence estimation of Williams syndrome.

Authors:  Petter Strømme; Per G Bjørnstad; Kjersti Ramstad
Journal:  J Child Neurol       Date:  2002-04       Impact factor: 1.987

10.  Cerebrovascular stenoses with cerebral infarction in a child with Williams syndrome.

Authors:  R H Ardinger; K K Goertz; L F Mattioli
Journal:  Am J Med Genet       Date:  1994-07-01
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  23 in total

1.  Klf15 deficiency is a molecular link between heart failure and aortic aneurysm formation.

Authors:  Saptarsi M Haldar; Yuan Lu; Darwin Jeyaraj; Daiji Kawanami; Yingjie Cui; Sam J Eapen; Caili Hao; Yan Li; Yong-Qiu Doughman; Michiko Watanabe; Koichi Shimizu; Helena Kuivaniemi; Junichi Sadoshima; Kenneth B Margulies; Thomas P Cappola; Mukesh K Jain
Journal:  Sci Transl Med       Date:  2010-04-07       Impact factor: 17.956

Review 2.  13q13.1-q13.2 deletion in tetralogy of Fallot: clinical report and a literature review.

Authors:  Gregory Costain; Candice K Silversides; Christian R Marshall; Mary Shago; Nicholas Costain; Anne S Bassett
Journal:  Int J Cardiol       Date:  2010-07-03       Impact factor: 4.164

Review 3.  CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes.

Authors:  Benjamin J Landis; David S Cooper; Robert B Hinton
Journal:  Cardiol Young       Date:  2015-09-08       Impact factor: 1.093

4.  Circulating mRNA in Maternal Plasma at the Second Trimester of Pregnancy: A Possible Screening Tool for Cardiac Conotruncal and Left Ventricular Outflow Tract Abnormalities.

Authors:  Elena Contro; Lara Stefani; Silvia Berto; Cristina Lapucci; Diego Arcelli; Daniela Prandstraller; Antonella Perolo; Nicola Rizzo; Antonio Farina
Journal:  Mol Diagn Ther       Date:  2017-12       Impact factor: 4.074

5.  New Genetic Insights into Congenital Heart Disease.

Authors:  Stephanie M Ware; John Lynn Jefferies
Journal:  J Clin Exp Cardiolog       Date:  2012-06-15

Review 6.  Genetic basis of congenital cardiovascular malformations.

Authors:  Seema R Lalani; John W Belmont
Journal:  Eur J Med Genet       Date:  2014-04-30       Impact factor: 2.708

Review 7.  Pulmonic Valve Disease: Review of Pathology and Current Treatment Options.

Authors:  Mouhammad Fathallah; Richard A Krasuski
Journal:  Curr Cardiol Rep       Date:  2017-09-16       Impact factor: 2.931

8.  Low-dose dasatinib rescues cardiac function in Noonan syndrome.

Authors:  Jae-Sung Yi; Yan Huang; Andrea T Kwaczala; Ivana Y Kuo; Barbara E Ehrlich; Stuart G Campbell; Frank J Giordano; Anton M Bennett
Journal:  JCI Insight       Date:  2016-12-08

9.  Massive-scale RNA-Seq analysis of non ribosomal transcriptome in human trisomy 21.

Authors:  Valerio Costa; Claudia Angelini; Luciana D'Apice; Margherita Mutarelli; Amelia Casamassimi; Linda Sommese; Maria Assunta Gallo; Marianna Aprile; Roberta Esposito; Luigi Leone; Aldo Donizetti; Stefania Crispi; Monica Rienzo; Berardo Sarubbi; Raffaele Calabrò; Marco Picardi; Paola Salvatore; Teresa Infante; Piergiuseppe De Berardinis; Claudio Napoli; Alfredo Ciccodicola
Journal:  PLoS One       Date:  2011-04-20       Impact factor: 3.240

10.  The Role of the Geneticist and Genetic Counselor in an ACHD Clinic.

Authors:  Ashley Parrott; Stephanie M Ware
Journal:  Prog Pediatr Cardiol       Date:  2012-07-12
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