Literature DB >> 3186348

Genetic disorders and major extracardiac anomalies associated with the hypoplastic left heart syndrome.

M Natowicz1, J Chatten, R Clancy, K Conard, T Glauser, D Huff, A Lin, W Norwood, L B Rorke, A Uri.   

Abstract

All pediatric autopsies of patients with hypoplastic left heart syndrome seen during an 11-year interval were reviewed to determine the frequency of underlying chromosomal and single-gene defects and idiopathic major extracardiac anomalies associated with this common, lethal congenital heart abnormality. Of 83 patients identified, nine had underlying chromosomal abnormalities, four had single-gene defects, ten had one or more major extracardiac anomalies without an identifiable chromosomal or mendelian disorder, and two were infants of insulin-dependent diabetic mothers. Overall, 23 patients (28%) had a genetic disorder and/or major extracardiac anomaly. The substantial prevalence of genetic causes of and major extracardiac anomalies associated with hypoplastic left heart syndrome underscores the need for a detailed genetic evaluation for all patients with hypoplastic left heart syndrome.

Entities:  

Mesh:

Year:  1988        PMID: 3186348

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


  13 in total

1.  Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome.

Authors:  Ashleigh R Payne; Sheng-Wei Chang; Sara N Koenig; Andrew R Zinn; Vidu Garg
Journal:  Pediatr Cardiol       Date:  2012-02-21       Impact factor: 1.655

Review 2.  Hypoplastic left heart syndrome: current considerations and expectations.

Authors:  Jeffrey A Feinstein; D Woodrow Benson; Anne M Dubin; Meryl S Cohen; Dawn M Maxey; William T Mahle; Elfriede Pahl; Juan Villafañe; Ami B Bhatt; Lynn F Peng; Beth Ann Johnson; Alison L Marsden; Curt J Daniels; Nancy A Rudd; Christopher A Caldarone; Kathleen A Mussatto; David L Morales; D Dunbar Ivy; J William Gaynor; James S Tweddell; Barbara J Deal; Anke K Furck; Geoffrey L Rosenthal; Richard G Ohye; Nancy S Ghanayem; John P Cheatham; Wayne Tworetzky; Gerard R Martin
Journal:  J Am Coll Cardiol       Date:  2012-01-03       Impact factor: 24.094

3.  Hypoplastic left heart syndrome with premature closure of foramen ovale: report of an unusual type of totally anomalous pulmonary venous return.

Authors:  K Suzuki; S Doi; K Oku; Y Murakami; K Mori; S Mimori; M Ando
Journal:  Heart Vessels       Date:  1990       Impact factor: 2.037

4.  Universal screening for extracardiac abnormalities in neonates with congenital heart disease.

Authors:  Javier H Gonzalez; Girish S Shirali; Andrew M Atz; Sarah N Taylor; Geoffrey A Forbus; Sinai C Zyblewski; Anthony M Hlavacek
Journal:  Pediatr Cardiol       Date:  2008-12-11       Impact factor: 1.655

5.  Hypoplastic left heart syndrome with male pseudohermaphroditism and bicornuate uterus bicollis.

Authors:  R D Calaluce; T H Huang; J T Quesenberry; M L Evans; A M Luger; T A O'Connor
Journal:  Pediatr Cardiol       Date:  1995 Sep-Oct       Impact factor: 1.655

6.  Prenatal head growth and white matter injury in hypoplastic left heart syndrome.

Authors:  Robert B Hinton; Gregor Andelfinger; Priya Sekar; Andrea C Hinton; Roxanne L Gendron; Erik C Michelfelder; Yves Robitaille; D Woodrow Benson
Journal:  Pediatr Res       Date:  2008-10       Impact factor: 3.756

7.  Cerebral hemorrhage and vasospasm in a child with congenital heart disease.

Authors:  Jessica Carpenter; Robert Keating; Steven Weinstein; Gilbert Vezina; John Berger; Michael J Bell
Journal:  Neurocrit Care       Date:  2008       Impact factor: 3.210

8.  Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart.

Authors:  Harinder K Gill; Sian R Parsons; Cosma Spalluto; Angela F Davies; Victoria J Knorz; Clare E G Burlinson; Bee Ling Ng; Nigel P Carter; Caroline Mackie Ogilvie; David I Wilson; Roland G Roberts
Journal:  Eur J Hum Genet       Date:  2009-05-27       Impact factor: 4.246

9.  Exploration and validation of hub genes and pathways in the progression of hypoplastic left heart syndrome via weighted gene co-expression network analysis.

Authors:  Xuelan Liu; Honglei Shang; Bin Li; Liyun Zhao; Ying Hua; Kaiyuan Wu; Manman Hu; Taibing Fan
Journal:  BMC Cardiovasc Disord       Date:  2021-06-15       Impact factor: 2.298

10.  A Homozygous Deletion of Exon 5 of KYNU Resulting from a Maternal Chromosome 2 Isodisomy (UPD2) Causes Catel-Manzke-Syndrome/VCRL Syndrome.

Authors:  Isabel Schüle; Urs Berger; Uta Matysiak; Gunda Ruzaike; Brigitte Stiller; Martin Pohl; Ute Spiekerkoetter; Ekkehart Lausch; Sarah C Grünert; Miriam Schmidts
Journal:  Genes (Basel)       Date:  2021-06-07       Impact factor: 4.096

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