Literature DB >> 16691589

New cases of Bohring-Opitz syndrome, update, and critical review of the literature.

Axel Bohring1, Grétel G Oudesluijs, Dorothy K Grange, Giuseppe Zampino, Patrick Thierry.   

Abstract

We report on four additional unrelated cases of Bohring-Opitz syndrome with the highly characteristic phenotype of facial anomalies including bulging forehead over the metopic suture, frontal nevus flammeus, exophthalmos, hypertelorism, upslanting palpebral fissures, and cleft lip and/or palate, as well as flexion deformities of the upper limbs, multiple other anomalies, and severe failure to thrive. We also update the clinical outcome of the patients reported in the original article by Bohring et al. [Am J Med Genet 85:438-446] and critically review the subsequently published cases considered to have Bohring-Opitz syndrome. Copyright 2006 Wiley-Liss, Inc.

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Year:  2006        PMID: 16691589     DOI: 10.1002/ajmg.a.31265

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


  8 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

Review 3.  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

4.  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

5.  Understanding the phenotypic spectrum of ASXL-related disease: Ten cases and a review of the literature.

Authors:  Vishnu Anand Cuddapah; Holly A Dubbs; Laura Adang; Steven L Kugler; Elizabeth M McCormick; Zarazuela Zolkipli-Cunningham; Xilma R Ortiz-González; Shana McCormack; Elaine Zackai; Daniel J Licht; Marni J Falk; Eric D Marsh
Journal:  Am J Med Genet A       Date:  2021-03-10       Impact factor: 2.578

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

7.  Novel compound heterozygous ASXL3 mutation causing Bainbridge-ropers like syndrome and primary IGF1 deficiency.

Authors:  Dinesh Giri; Daniel Rigden; Mohammed Didi; Matthew Peak; Paul McNamara; Senthil Senniappan
Journal:  Int J Pediatr Endocrinol       Date:  2017-08-04

8.  Bohring-Opitz syndrome caused by a novel ASXL1 mutation (c.3762delT) in an IVF baby: A case report.

Authors:  Dongbo Wang; Xin Yuan; Haichun Guo; Shuyuan Yan; Guohong Wang; Yanling Wang; Tuanmei Wang; Jun He; Xiangwen Peng
Journal:  Medicine (Baltimore)       Date:  2022-02-04       Impact factor: 1.817

  8 in total

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