Literature DB >> 12923867

Donnai-Barrow syndrome: four additional patients.

Nicolas Chassaing1, Didier Lacombe, Dominique Carles, Patrick Calvas, Robert Saura, Eric Bieth.   

Abstract

In 1993, Donnai and Barrow reported a new syndrome in two sets of sibs and in an unrelated child, including diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, and sensorineural deafness. Since then, only four similar patients have been documented. We describe four additional patients, including two sibling pairs from healthy parents. This report firmly establishes this syndrome as a distinct clinical entity and provides further evidence for its previously postulated autosomal recessive inheritance. Copyright 2003 Wiley-Liss, Inc.

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Year:  2003        PMID: 12923867     DOI: 10.1002/ajmg.a.20266

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  8 in total

1.  Assessment and Treatment of Self-Injurious Behavior Associated with Donnai-Barrow Syndrome.

Authors:  Henry Roane; Kelly Bouxsein; Caitlin Fulton
Journal:  J Dev Phys Disabil       Date:  2012-08

Review 2.  Review of the evidence on the closure of abdominal wall defects.

Authors:  Vincent E Mortellaro; Shawn D St Peter; Frankie B Fike; Saleem Islam
Journal:  Pediatr Surg Int       Date:  2010-12-14       Impact factor: 1.827

Review 3.  Overview of epidemiology, genetics, birth defects, and chromosome abnormalities associated with CDH.

Authors:  Barbara R Pober
Journal:  Am J Med Genet C Semin Med Genet       Date:  2007-05-15       Impact factor: 3.908

Review 4.  A review of Donnai-Barrow and facio-oculo-acoustico-renal (DB/FOAR) syndrome: clinical features and differential diagnosis.

Authors:  Barbara R Pober; Mauro Longoni; Kristin M Noonan
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2009-01

Review 5.  Genetic aspects of human congenital diaphragmatic hernia.

Authors:  B R Pober
Journal:  Clin Genet       Date:  2008-05-28       Impact factor: 4.438

6.  Investigation of TBR1 Hemizygosity: Four Individuals with 2q24 Microdeletions.

Authors:  R N Traylor; W B Dobyns; J A Rosenfeld; P Wheeler; J E Spence; A M Bandholz; E V Bawle; E P Carmany; C M Powell; B Hudson; R A Schultz; L G Shaffer; B C Ballif
Journal:  Mol Syndromol       Date:  2012-08-23

7.  Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes.

Authors:  Sibel Kantarci; Lihadh Al-Gazali; R Sean Hill; Dian Donnai; Graeme C M Black; Eric Bieth; Nicolas Chassaing; Didier Lacombe; Koen Devriendt; Ahmad Teebi; Maria Loscertales; Caroline Robson; Tianming Liu; David T MacLaughlin; Kristin M Noonan; Meaghan K Russell; Christopher A Walsh; Patricia K Donahoe; Barbara R Pober
Journal:  Nat Genet       Date:  2007-07-15       Impact factor: 38.330

Review 8.  Management of Congenital Diaphragmatic Hernia (CDH): Role of Molecular Genetics.

Authors:  Giulia Cannata; Chiara Caporilli; Federica Grassi; Serafina Perrone; Susanna Esposito
Journal:  Int J Mol Sci       Date:  2021-06-14       Impact factor: 5.923

  8 in total

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