Literature DB >> 17436238

Genetic factors in congenital diaphragmatic hernia.

A M Holder1, M Klaassens, D Tibboel, A de Klein, B Lee, D A Scott.   

Abstract

Congenital diaphragmatic hernia (CDH) is a relatively common birth defect associated with high mortality and morbidity. Although the exact etiology of most cases of CDH remains unknown, there is a growing body of evidence that genetic factors play an important role in the development of CDH. In this review, we examine key findings that are likely to form the basis for future research in this field. Specific topics include a short overview of normal and abnormal diaphragm development, a discussion of syndromic forms of CDH, a detailed review of chromosomal regions recurrently altered in CDH, a description of the retinoid hypothesis of CDH, and evidence of the roles of specific genes in the development of CDH.

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Year:  2007        PMID: 17436238      PMCID: PMC1852742          DOI: 10.1086/513442

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  177 in total

1.  A family with a grand-maternally derived interstitial duplication of proximal 15q.

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Journal:  Clin Genet       Date:  2001-12       Impact factor: 4.438

2.  A fetus with pseudo Fryns syndrome and t(18;22) translocation.

Authors:  A Geneix; J Goburdhun; C Fallet; G Lacroute; D Satge
Journal:  Genet Couns       Date:  2001

3.  Prenatal findings for complete trisomy 9.

Authors:  Nobuhiro Suzumori; Takeshi Sato; Junko Okada; Tamao Nakanishi; Kenji Shirai; Mitsuyo Tanemura; Yoshikatsu Suzuki; Kaoru Suzumori
Journal:  Prenat Diagn       Date:  2003-10       Impact factor: 3.050

4.  Terminal deletion of 6q and Fryns syndrome: a microdeletion/syndrome pair?

Authors:  N Krassikoff; G S Sekhon
Journal:  Am J Med Genet       Date:  1990-07

5.  A case of mosaic tetrasomy 12p (Pallister-Killian Syndrome) diagnosed prenatally: comparison of chromosome analyses of various cells obtained from the patient.

Authors:  K Takakuwa; I Hataya; M Arakawa; M Tamura; N Sekizuka; K Tanaka
Journal:  Am J Perinatol       Date:  1997-11       Impact factor: 1.862

6.  Tissue-specific mosaicism among fetuses with prenatally diagnosed diaphragmatic hernia.

Authors:  A E Donnenfeld; T J Campbell; J Byers; R J Librizzi; S Weiner
Journal:  Am J Obstet Gynecol       Date:  1993-10       Impact factor: 8.661

7.  Trisomy 22 in an Iowa newborn.

Authors:  S Golombek; R Shaw
Journal:  Iowa Med       Date:  1994-01

8.  Congenital diaphragmatic hernia in a patient with tetrasomy 9p.

Authors:  Tiago Henriques-Coelho; Natália Oliva-Teles; M Luz Fonseca-Silva; Dick Tibboel; Hercília Guimarães; Jorge Correia-Pinto
Journal:  J Pediatr Surg       Date:  2005-10       Impact factor: 2.545

9.  Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization.

Authors:  M Klaassens; M van Dooren; H J Eussen; H Douben; A T den Dekker; C Lee; P K Donahoe; R J Galjaard; N Goemaere; R R de Krijger; C Wouters; J Wauters; B A Oostra; D Tibboel; A de Klein
Journal:  Am J Hum Genet       Date:  2005-03-04       Impact factor: 11.025

10.  Diaphragmatic herniae and translocations involving 8q22 in two patients.

Authors:  I K Temple; J C Barber; R S James; D Burge
Journal:  J Med Genet       Date:  1994-09       Impact factor: 6.318

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  60 in total

1.  Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemia.

Authors:  Margaret J Wat; Victoria B Enciso; Wojciech Wiszniewski; Trevor Resnick; Patricia Bader; Elizabeth R Roeder; Debra Freedenberg; Chester Brown; Pawel Stankiewicz; Sau-Wai Cheung; Daryl A Scott
Journal:  J Med Genet       Date:  2010-10-04       Impact factor: 6.318

2.  Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts.

Authors:  Danielle Veenma; Erwin Brosens; Elisabeth de Jong; Cees van de Ven; Connie Meeussen; Titia Cohen-Overbeek; Marjan Boter; Hubertus Eussen; Hannie Douben; Dick Tibboel; Annelies de Klein
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

3.  Expression of the Wilm's tumor gene WT1 during diaphragmatic development in the nitrofen model for congenital diaphragmatic hernia.

Authors:  Jens Dingemann; Takashi Doi; Elke Ruttenstock; Prem Puri
Journal:  Pediatr Surg Int       Date:  2011-02       Impact factor: 1.827

4.  Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1.

Authors:  Margaret J Wat; Tyler F Beck; Andrés Hernández-García; Zhiyin Yu; Danielle Veenma; Monica Garcia; Ashley M Holder; Jeanette J Wat; Yuqing Chen; Carrie A Mohila; Kevin P Lally; Mary Dickinson; Dick Tibboel; Annelies de Klein; Brendan Lee; Daryl A Scott
Journal:  Hum Mol Genet       Date:  2012-06-20       Impact factor: 6.150

5.  Deletions of Xp provide evidence for the role of holocytochrome C-type synthase (HCCS) in congenital diaphragmatic hernia.

Authors:  Kanwal Qidwai; David M Pearson; Gayle Simpson Patel; Barbara R Pober; Ladonna L Immken; Sau Wai Cheung; Daryl A Scott
Journal:  Am J Med Genet A       Date:  2010-06       Impact factor: 2.802

6.  Unruptured sinus of Valsalva aneurysm presenting with concurrent Morgagni hernia.

Authors:  Jonathan J Masor; S Scott Davis; Edward P Chen; Travis S Henry; Wendy M Book
Journal:  Proc (Bayl Univ Med Cent)       Date:  2015-10

7.  Congenital diaphragmatic hernia candidate genes derived from embryonic transcriptomes.

Authors:  Meaghan K Russell; Mauro Longoni; Julie Wells; Faouzi I Maalouf; Adam A Tracy; Maria Loscertales; Kate G Ackerman; Barbara R Pober; Kasper Lage; Carol J Bult; Patricia K Donahoe
Journal:  Proc Natl Acad Sci U S A       Date:  2012-02-06       Impact factor: 11.205

8.  Roundabout receptors are critical for foregut separation from the body wall.

Authors:  Eric Thomas Domyan; Kelsey Branchfield; Daniel A Gibson; L A Naiche; Mark Lewandoski; Marc Tessier-Lavigne; Le Ma; Xin Sun
Journal:  Dev Cell       Date:  2013-01-14       Impact factor: 12.270

9.  Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.

Authors:  Tyler F Beck; Danielle Veenma; Oleg A Shchelochkov; Zhiyin Yu; Bum Jun Kim; Hitisha P Zaveri; Yolande van Bever; Sunju Choi; Hannie Douben; Terry K Bertin; Pragna I Patel; Brendan Lee; Dick Tibboel; Annelies de Klein; David W Stockton; Monica J Justice; Daryl A Scott
Journal:  Hum Mol Genet       Date:  2012-12-05       Impact factor: 6.150

10.  Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia.

Authors:  Margaret J Wat; Oleg A Shchelochkov; Ashley M Holder; Amy M Breman; Aditi Dagli; Carlos Bacino; Fernando Scaglia; Roberto T Zori; Sau Wai Cheung; Daryl A Scott; Sung-Hae Lee Kang
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

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