Literature DB >> 25790323

Review of X-linked syndromes with arthrogryposis or early contractures-aid to diagnosis and pathway identification.

Jesse M Hunter1, Jeff Kiefer, Christopher D Balak, Sonya Jooma, Mary Ellen Ahearn, Judith G Hall, Lisa Baumbach-Reardon.   

Abstract

The following is a review of 50 X-linked syndromes and conditions associated with either arthrogryposis or other types of early contractures. These entities are categorized as those with known responsible gene mutations, those which are definitely X-linked, but the responsible gene has not been identified, and those suspected from family history to be X-linked. Several important ontology pathways for known disease genes have been identified and are discussed in relevance to clinical characteristics. Tables are included which help to identify distinguishing clinical features of each of the conditions.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  X-linked; arthrogryposis; arthrogryposis multiplex congenita; contractures; multiple congenital contractures; myopathy; spinal muscular atrophy

Mesh:

Year:  2015        PMID: 25790323     DOI: 10.1002/ajmg.a.36934

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


  8 in total

1.  Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin.

Authors:  Yavuz Bayram; Ender Karaca; Zeynep Coban Akdemir; Elif Ozdamar Yilmaz; Gulsen Akay Tayfun; Hatip Aydin; Deniz Torun; Sevcan Tug Bozdogan; Alper Gezdirici; Sedat Isikay; Mehmed M Atik; Tomasz Gambin; Tamar Harel; Ayman W El-Hattab; Wu-Lin Charng; Davut Pehlivan; Shalini N Jhangiani; Donna M Muzny; Ali Karaman; Tamer Celik; Ozge Ozalp Yuregir; Timur Yildirim; Ilhan A Bayhan; Eric Boerwinkle; Richard A Gibbs; Nursel Elcioglu; Beyhan Tuysuz; James R Lupski
Journal:  J Clin Invest       Date:  2016-01-11       Impact factor: 14.808

Review 2.  Arthrogryposis as a Syndrome: Gene Ontology Analysis.

Authors:  Judith G Hall; Jeff Kiefer
Journal:  Mol Syndromol       Date:  2016-06-07

3.  Perspective: Modulating the integrated stress response to slow aging and ameliorate age-related pathology.

Authors:  Maxime J Derisbourg; Matías D Hartman; Martin S Denzel
Journal:  Nat Aging       Date:  2021-09-13

4.  Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita.

Authors:  Suzanna G M Frints; Friederike Hennig; Roberto Colombo; Sebastien Jacquemont; Paulien Terhal; Holly H Zimmerman; David Hunt; Bryce A Mendelsohn; Ulrike Kordaß; Richard Webster; Margje Sinnema; Omar Abdul-Rahman; Vanessa Suckow; Alberto Fernández-Jaén; Kees van Roozendaal; Servi J C Stevens; Merryn V E Macville; Salwan Al-Nasiry; Koen van Gassen; Norbert Utzig; Suzanne M Koudijs; Lesley McGregor; Saskia M Maas; Diana Baralle; Abhijit Dixit; Peter Wieacker; Marcus Lee; Arthur S Lee; Elizabeth C Engle; Gunnar Houge; Gyri A Gradek; Andrew G L Douglas; Cheryl Longman; Shelagh Joss; Danita Velasco; Raoul C Hennekam; Hiromi Hirata; Vera M Kalscheuer
Journal:  Hum Mutat       Date:  2019-08-21       Impact factor: 4.878

5.  A novel Xp11.22-22.33 deletion suggesting a possible mechanism of congenital cervical spinal muscular atrophy.

Authors:  Jingwei Liu; Kelai Wang; Baomin Li; Xiaofan Yang
Journal:  Mol Genet Genomic Med       Date:  2021-01-29       Impact factor: 2.183

6.  MET mutation causes muscular dysplasia and arthrogryposis.

Authors:  Hang Zhou; Chengjie Lian; Tingting Wang; Xiaoming Yang; Caixia Xu; Deying Su; Shuhui Zheng; Xiangyu Huang; Zhiheng Liao; Taifeng Zhou; Xianjian Qiu; Yuyu Chen; Bo Gao; Yongyong Li; Xudong Wang; Guoling You; Qihua Fu; Christina Gurnett; Dongsheng Huang; Peiqiang Su
Journal:  EMBO Mol Med       Date:  2019-03       Impact factor: 12.137

7.  Development of a research platform for children with arthrogryposis multiplex congenita: study protocol for a pilot registry.

Authors:  Noémi Dahan-Oliel; Tanya Bedard; Vasiliki Betty Darsaklis; Judith Goslin Hall; Harold J P van Bosse; Reggie C Hamdy
Journal:  BMJ Open       Date:  2018-06-30       Impact factor: 2.692

8.  A novel de novo nonsense mutation in ZC4H2 causes Wieacker-Wolff Syndrome.

Authors:  Dan Wang; Dongjie Hu; Zhichao Guo; Rong Hu; Qunxian Wang; Yannan Liu; Mingjing Liu; Zijun Meng; Huan Yang; Yun Zhang; Fang Cai; Weihui Zhou; Weihong Song
Journal:  Mol Genet Genomic Med       Date:  2019-12-30       Impact factor: 2.183

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.