Literature DB >> 20541044

A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings.

Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Wen-Ling Chen, Wayseen Wang.   

Abstract

We report a 5-year-old boy with mental retardation, autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings, carrying a 7.9 Mb de novo deletion of chromosome 22q13.2→qter. This region contains the SHANK3, NCAPH2 and CYP2D6 genes which are associated with T-cell immune response. The present case provides evidence that 22q13 deletion syndrome may be associated with immune system dysfunction in addition to neuropsychiatric disorders.
Copyright © 2010 Elsevier Masson SAS. All rights reserved.

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Year:  2010        PMID: 20541044     DOI: 10.1016/j.ejmg.2010.06.004

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  12 in total

Review 1.  Distribution of disease-associated copy number variants across distinct disorders of cognitive development.

Authors:  Matthew F Pescosolido; Ece D Gamsiz; Shailender Nagpal; Eric M Morrow
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2013-04       Impact factor: 8.829

2.  Identifying CNVs in 15q11q13 and 16p11.2 of Patients with Seizures Increases the Rates of Detecting Pathogenic Changes.

Authors:  Gabrielle S Vianna; Mariana L Freitas; Valdirene T de Oliveira; Rafaella X Pietra; Michele da S Gonçalves; Patrícia P O Rocha; Rejane A C Monteiro; Luana C A Ferreira; Rosana R Xavier; Andréia M Carvalho; Patrícia R de M Lima; Maria Augusta N P Monteiro; Elvis C Mateo; Juliana G Giannetti; Giovana da C César; Joziele de S Lima; Paula F V Medeiros; Fernanda S Jehee
Journal:  Mol Syndromol       Date:  2016-11-01

3.  Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits.

Authors:  Haley E Speed; Mehreen Kouser; Zhong Xuan; Jeremy M Reimers; Christine F Ochoa; Natasha Gupta; Shunan Liu; Craig M Powell
Journal:  J Neurosci       Date:  2015-07-01       Impact factor: 6.167

4.  Transfer RNA-derived fragment tRF-28-QSZ34KRQ590K in plasma exosomes may be a potential biomarker for atopic dermatitis in pediatric patients.

Authors:  Li Meng; Long Jiang; Jian Chen; Hongjin Ren; Zhiqin Gao; Fei Wu; Yiyang Wen; Lianjuan Yang
Journal:  Exp Ther Med       Date:  2021-03-16       Impact factor: 2.447

Review 5.  Glutamatergic candidate genes in autism spectrum disorder: an overview.

Authors:  Andreas G Chiocchetti; Hanna S Bour; Christine M Freitag
Journal:  J Neural Transm (Vienna)       Date:  2014-02-04       Impact factor: 3.575

6.  Association between atopic diseases and neurodevelopmental disabilities in a longitudinal birth cohort.

Authors:  Xueqi Qu; Li-Ching Lee; Christine Ladd-Acosta; Xiumei Hong; Yuelong Ji; Luther G Kalb; Heather E Volk; Xiaobin Wang
Journal:  Autism Res       Date:  2022-02-02       Impact factor: 5.216

Review 7.  Phelan-McDermid syndrome: a review of the literature and practice parameters for medical assessment and monitoring.

Authors:  Alexander Kolevzon; Benjamin Angarita; Lauren Bush; A Ting Wang; Yitzchak Frank; Amy Yang; Robert Rapaport; Jeffrey Saland; Shubhika Srivastava; Cristina Farrell; Lisa J Edelmann; Joseph D Buxbaum
Journal:  J Neurodev Disord       Date:  2014-10-08       Impact factor: 4.025

8.  Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.

Authors:  Latha Soorya; Alexander Kolevzon; Jessica Zweifach; Teresa Lim; Yuriy Dobry; Lily Schwartz; Yitzchak Frank; A Ting Wang; Guiqing Cai; Elena Parkhomenko; Danielle Halpern; David Grodberg; Benjamin Angarita; Judith P Willner; Amy Yang; Roberto Canitano; William Chaplin; Catalina Betancur; Joseph D Buxbaum
Journal:  Mol Autism       Date:  2013-06-11       Impact factor: 7.509

9.  A new locus on chromosome 22q13.31 linked to recessive genetic epilepsy with febrile seizures plus (GEFS+) in a Tunisian consanguineous family.

Authors:  Nejla Belhedi; Frédérique Bena; Amel Mrabet; Michel Guipponi; Chiraz Bouchlaka Souissi; Hela Khiari Mrabet; Amel Benammar Elgaaied; Alain Malafosse; Annick Salzmann
Journal:  BMC Genet       Date:  2013-09-25       Impact factor: 2.797

10.  Chromothripsis and ring chromosome 22: a paradigm of genomic complexity in the Phelan-McDermid syndrome (22q13 deletion syndrome).

Authors:  Nehir Kurtas; Filippo Arrigoni; Edoardo Errichiello; Claudio Zucca; Cristina Maghini; Maria Grazia D'Angelo; Silvana Beri; Roberto Giorda; Sara Bertuzzo; Massimo Delledonne; Luciano Xumerle; Marzia Rossato; Orsetta Zuffardi; Maria Clara Bonaglia
Journal:  J Med Genet       Date:  2018-01-29       Impact factor: 6.318

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