Literature DB >> 29254829

A severe female case of arthrogryposis multiplex congenita with brain atrophy, spastic quadriplegia and intellectual disability caused by ZC4H2 mutation.

Yukimune Okubo1, Wakaba Endo2, Takehiko Inui3, Sato Suzuki-Muromoto3, Takuya Miyabayashi3, Noriko Togashi3, Ryo Sato3, Natsuko Arai-Ichinoi2, Atsuo Kikuchi2, Shigeo Kure2, Kazuhiro Haginoya3.   

Abstract

Arthrogryposis multiplex congenita (AMC) is characterized by heterogeneous multiple congenital contractures appearing at birth. Mutations in X-linked zinc-finger gene ZC4H2 were recently identified in some families and individuals with variable forms of AMC associated with dysmorphic signs, intellectual disability and spastic paresis. We present a non-consanguineous Japanese female presenting AMC with severe intellectual disability and spastic quadriplegia who also had progressive brain atrophy. Microarray-based comparative genomic hybridization identified 395 kb microdeletions at Xq11.2 which only included ZC4H2 gene. Previous reports showed that affected females have lesser symptoms and slight abnormality on brain MRI compared to male due to X-inactivation. Our case, however, showed severe manifestation than as ever reported as well as progressive diffuse brain atrophy, which implicated contribution of other genetic or environmental factors or extremely skewed X inactivation.
Copyright © 2017 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Arthrogryposis multiplex congenita (AMC); Progressive brain atrophy; Spastic quadriplegia; X-inactivation; ZC4H2

Mesh:

Substances:

Year:  2017        PMID: 29254829     DOI: 10.1016/j.braindev.2017.11.011

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  4 in total

1.  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

2.  ZC4H2 stabilizes RNF220 to pattern ventral spinal cord through modulating Shh/Gli signaling.

Authors:  Pengcheng Ma; Ning-Ning Song; Xiaoning Cheng; Liang Zhu; Qiong Zhang; Long Long Zhang; Xiangcai Yang; Huishan Wang; Qinghua Kong; Deli Shi; Yu-Qiang Ding; Bingyu Mao
Journal:  J Mol Cell Biol       Date:  2020-06-11       Impact factor: 6.216

3.  Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene.

Authors:  Jing-Jing Sun; Qin Cai; Miao Xu; Yan-Na Liu; Wan-Rui Li; Juan Li; Li Ma; Cheng Cai; Xiao-Hui Gong; Yi-Tao Zeng; Zhao-Rui Ren; Fanyi Zeng
Journal:  Genes (Basel)       Date:  2022-08-29       Impact factor: 4.141

4.  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

  4 in total

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