Literature DB >> 21368916

Bohring-Opitz (Oberklaid-Danks) syndrome: clinical study, review of the literature, and discussion of possible pathogenesis.

Rob Hastings1, Jan-Maarten Cobben, Gabriele Gillessen-Kaesbach, Judith Goodship, Hanne Hove, Susanne Kjaergaard, Helena Kemp, Helen Kingston, Peter Lunt, Sahar Mansour, Ruth McGowan, Kay Metcalfe, Catherine Murdoch-Davis, Mary Ray, Marlène Rio, Sarah Smithson, John Tolmie, Peter Turnpenny, Bregje van Bon, Dagmar Wieczorek, Ruth Newbury-Ecob.   

Abstract

Bohring-Opitz syndrome (BOS) is a rare congenital disorder of unknown etiology diagnosed on the basis of distinctive clinical features. We suggest diagnostic criteria for this condition, describe ten previously unreported patients, and update the natural history of four previously reported patients. This is the largest series reported to date, providing a unique opportunity to document the key clinical features and course through childhood. Investigations undertaken to try and elucidate the underlying pathogenesis of BOS using array comparative genomic hybridization and tandem mass spectrometry of cholesterol precursors did not show any pathogenic changes responsible.

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Year:  2011        PMID: 21368916      PMCID: PMC3083618          DOI: 10.1038/ejhg.2010.234

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  11 in total

1.  The Opitz trigonocephaly syndrome. A case report.

Authors:  F Oberklaid; D M Danks
Journal:  Am J Dis Child       Date:  1975-11

2.  Evolution of a patient with Bohring-Opitz syndrome.

Authors:  Sophie Pierron; Christian Richelme; Valérie Triolo; Jean Christophe Mas; Jacques Griffet; Houda Karmous-Benailly; M Quere; Tadashi Kaname; Jean-Claude Lambert; Fabienne Giuliano
Journal:  Am J Med Genet A       Date:  2009-08       Impact factor: 2.802

3.  Opitz trigonocephaly C syndrome in a boy with a de novo balanced reciprocal translocation t(3;18)(q13.13;q12.1).

Authors:  Yasutsugu Chinen; Tadashi Kaname; Kumiko Yanagi; Nakamichi Saito; Kenji Naritomi; Takao Ohta
Journal:  Am J Med Genet A       Date:  2006-08-01       Impact factor: 2.802

Review 4.  Severe end of Opitz trigonocephaly (C) syndrome or new syndrome?

Authors:  A Bohring; M Silengo; M Lerone; D W Superneau; C Spaich; S R Braddock; A Poss; J M Opitz
Journal:  Am J Med Genet       Date:  1999-08-27

5.  Trisomy of 3pter in a patient with apparent C (trigonocephaly) syndrome.

Authors:  J McGaughran; S Aftimos; P Oei
Journal:  Am J Med Genet       Date:  2000-10-02

6.  "C" trigonocephaly syndrome with diaphragmnatic hernia.

Authors:  M C Addor; D Stefanutti; F Farron; P Meinecke; D Lacombe; J Sarlangue; G Prescia; D F Schorderet
Journal:  Genet Couns       Date:  1995

7.  Infantile high myopia in Bohring-Opitz syndrome.

Authors:  Andrew R H Simpson; Caspar E A Gibbon; Anthony G Quinn; Peter D Turnpenny
Journal:  J AAPOS       Date:  2007-05-10       Impact factor: 1.220

8.  Transmitted cytogenetic abnormalities in patients with mental retardation: pathogenic or normal variants?

Authors:  Anne-Marie Bisgaard; Maria Kirchhoff; Jens Erik Nielsen; Carsten Brandt; Hanne Hove; Birgit Jepsen; Tim Jensen; Reinhard Ullmann; Flemming Skovby
Journal:  Eur J Med Genet       Date:  2007-04-14       Impact factor: 2.708

9.  Diagnosis of Smith-Lemli-Opitz syndrome by gas chromatography/mass spectrometry of 7-dehydrocholesterol in plasma, amniotic fluid and cultured skin fibroblasts.

Authors:  R I Kelley
Journal:  Clin Chim Acta       Date:  1995-04-30       Impact factor: 3.786

10.  Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome.

Authors:  Tadashi Kaname; Kumiko Yanagi; Yasutsugu Chinen; Yoshio Makita; Nobuhiko Okamoto; Hiroki Maehara; Ichiro Owan; Fuminori Kanaya; Yoshiaki Kubota; Yuichi Oike; Toshiyuki Yamamoto; Kenji Kurosawa; Yoshimitsu Fukushima; Axel Bohring; John M Opitz; Ko-Ichiro Yoshiura; Norio Niikawa; Kenji Naritomi
Journal:  Am J Hum Genet       Date:  2007-08-27       Impact factor: 11.025

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  13 in total

1.  De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome.

Authors:  Alexander Hoischen; Bregje W M van Bon; Benjamín Rodríguez-Santiago; Christian Gilissen; Lisenka E L M Vissers; Petra de Vries; Irene Janssen; Bart van Lier; Rob Hastings; Sarah F Smithson; Ruth Newbury-Ecob; Susanne Kjaergaard; Judith Goodship; Ruth McGowan; Deborah Bartholdi; Anita Rauch; Maarit Peippo; Jan M Cobben; Dagmar Wieczorek; Gabriele Gillessen-Kaesbach; Joris A Veltman; Han G Brunner; Bert B B A de Vries
Journal:  Nat Genet       Date:  2011-06-26       Impact factor: 38.330

2.  Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillance.

Authors:  Bianca Russell; Jennifer J Johnston; Leslie G Biesecker; Nancy Kramer; Angela Pickart; William Rhead; Wen-Hann Tan; Catherine A Brownstein; L Kate Clarkson; Amy Dobson; Avi Z Rosenberg; Samantha A Schrier Vergano; Benjamin M Helm; Rachel E Harrison; John M Graham
Journal:  Am J Med Genet A       Date:  2015-04-29       Impact factor: 2.802

3.  Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition.

Authors:  Alma Kuechler; Johanna Christina Czeschik; Elisabeth Graf; Ute Grasshoff; Ulrike Hüffmeier; Tiffany Busa; Stefanie Beck-Woedl; Laurence Faivre; Jean-Baptiste Rivière; Ingrid Bader; Johannes Koch; André Reis; Ute Hehr; Olaf Rittinger; Wolfgang Sperl; Tobias B Haack; Thomas Wieland; Hartmut Engels; Holger Prokisch; Tim M Strom; Hermann-Josef Lüdecke; Dagmar Wieczorek
Journal:  Eur J Hum Genet       Date:  2016-11-30       Impact factor: 4.246

Review 4.  Germline Abnormalities in DNA Methylation and Histone Modification and Associated Cancer Risk.

Authors:  Jenna A Fernandez; Mrinal M Patnaik
Journal:  Curr Hematol Malig Rep       Date:  2022-06-02       Impact factor: 4.213

Review 5.  Surveillance Recommendations for Children with Overgrowth Syndromes and Predisposition to Wilms Tumors and Hepatoblastoma.

Authors:  Jennifer M Kalish; Leslie Doros; Lee J Helman; Raoul C Hennekam; Roland P Kuiper; Saskia M Maas; Eamonn R Maher; Kim E Nichols; Sharon E Plon; Christopher C Porter; Surya Rednam; Kris Ann P Schultz; Lisa J States; Gail E Tomlinson; Kristin Zelley; Todd E Druley
Journal:  Clin Cancer Res       Date:  2017-07-01       Impact factor: 12.531

6.  Loss of Asxl1 Alters Self-Renewal and Cell Fate of Bone Marrow Stromal Cell, Leading to Bohring-Opitz-like Syndrome in Mice.

Authors:  Peng Zhang; Caihong Xing; Steven D Rhodes; Yongzheng He; Kai Deng; Zhaomin Li; Fuhong He; Caiying Zhu; Lihn Nguyen; Yuan Zhou; Shi Chen; Khalid S Mohammad; Theresa A Guise; Omar Abdel-Wahab; Mingjiang Xu; Qian-Fei Wang; Feng-Chun Yang
Journal:  Stem Cell Reports       Date:  2016-05-26       Impact factor: 7.765

Review 7.  Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples.

Authors:  Marcella Zollino; Serena Lattante; Daniela Orteschi; Silvia Frangella; Paolo N Doronzio; Ilaria Contaldo; Eugenio Mercuri; Giuseppe Marangi
Journal:  Front Neurosci       Date:  2017-10-18       Impact factor: 4.677

8.  De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome.

Authors:  Matthew N Bainbridge; Hao Hu; Donna M Muzny; Luciana Musante; James R Lupski; Brett H Graham; Wei Chen; Karen W Gripp; Kim Jenny; Thomas F Wienker; Yaping Yang; V Reid Sutton; Richard A Gibbs; H Hilger Ropers
Journal:  Genome Med       Date:  2013-02-05       Impact factor: 11.117

9.  De novo frameshift mutation in ASXL3 in a patient with global developmental delay, microcephaly, and craniofacial anomalies.

Authors:  Darrell L Dinwiddie; Sarah E Soden; Carol J Saunders; Neil A Miller; Emily G Farrow; Laurie D Smith; Stephen F Kingsmore
Journal:  BMC Med Genomics       Date:  2013-09-17       Impact factor: 3.063

10.  Autoimmune Hepatitis with Distal Renal Tubular Acidosis and Small Bowel Partial Malrotation.

Authors:  Tejas Kanaiyalal Modi; Hardik Parikh; Abhishek Sadalge; Amit Gupte; Pratin Bhatt; Akash Shukla
Journal:  Euroasian J Hepatogastroenterol       Date:  2016-07-09
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