Literature DB >> 15581841

Large duplication 4q25-q34 with mild clinical effect.

Hatem Elghezal1, Halima Sennana Sendi, Kamel Monastiri, Jean Michel Lapierre, Samira Ibala Romdhane, Soumaya Mougou, Ali Saad.   

Abstract

We report on a 5-year-old Tunisian boy with particular dysmorphic features and mild mental retardation limited in delayed and poor language acquisition. Cytogenetic analysis using RHG banding and FISH using whole chromosome four painting probe showed a partial duplication in the long arm of chromosome four. Locus specific probes and CGH confirmed the presence of a ''pure'' partial trisomy 4q due to de novo direct tandem dup(4)(q25q34). Comparative analysis of our case with those published previously, suggests that region 4q31-q33 may be involved in the development of the 4q characteristic dysmorphic features and the distal band 4q35 may be involved in the development of microcephaly and severe mental and growth retardation.

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Year:  2004        PMID: 15581841     DOI: 10.1016/j.anngen.2004.07.007

Source DB:  PubMed          Journal:  Ann Genet        ISSN: 0003-3995


  7 in total

1.  Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicism.

Authors:  Lucie Tosca; Sophie Brisset; François M Petit; Laure Lecerf; Ghislaine Rousseau; Cécile Bas; Mireille Laroudie; Marie-Laure Maurin; Sylvie Tapia; Olivier Picone; Sophie Prevot; Michel Goossens; Philippe Labrune; Gérard Tachdjian
Journal:  Eur J Hum Genet       Date:  2010-04-28       Impact factor: 4.246

2.  A novel 5p15.33-14.1 deletion and 4q34.24-35.2 duplication in a patient with mental retardation, dysmorphic features and severe speech delay.

Authors:  Qinying Cao; Yuanyuan Peng; Jun Ge; Yanhua Zhang; Junzhen Zhu; Lijuan Zhao
Journal:  J Genet       Date:  2014-04       Impact factor: 1.166

3.  Duplication of intrachromosomal insertion segments 4q32→q35 confirmed by comparative genomic hybridization and fluorescent in situ hybridization.

Authors:  Jin Woo Kim; Ju Yeon Park; Ah Rum Oh; Eun Young Choi; Hyun Mee Ryu; Inn Soo Kang; Mi Kyoung Koong; So Yeon Park
Journal:  Clin Exp Reprod Med       Date:  2011-12-31

4.  Partial trisomy 4q and monosomy 5p inherited from a maternal translocationt(4;5)(q33; p15) in three adverse pregnancies.

Authors:  Jingbo Zhang; Bei Zhang; Tong Liu; Huihui Xie; Jingfang Zhai
Journal:  Mol Cytogenet       Date:  2020-06-30       Impact factor: 2.009

Review 5.  Clinical, cytogenetic, and molecular findings in a fetus with ultrasonic multiple malformations, 4q duplication, and 7q deletion: A case report and literature review.

Authors:  Fagui Yue; Yuting Jiang; Yang Yu; Xiao Yang; Hongguo Zhang; Ruizhi Liu; Ruixue Wang
Journal:  Medicine (Baltimore)       Date:  2018-11       Impact factor: 1.889

6.  Case Report: Phenotype-Gene Correlation in a Case of Novel Tandem 4q Microduplication With Short Stature, Speech Delay and Microcephaly.

Authors:  Umm-Kulthum Ismail Umlai; Basma Haris; Khalid Hussain; Puthen Veettil Jithesh
Journal:  Front Endocrinol (Lausanne)       Date:  2022-02-03       Impact factor: 5.555

7.  Gain of chromosome 4qter and loss of 5pter: an unusual case with features of cri du chat syndrome.

Authors:  Frenny Sheth; Naresh Gohel; Thomas Liehr; Olakanmi Akinde; Manisha Desai; Olawaleye Adeteye; Jayesh Sheth
Journal:  Case Rep Genet       Date:  2012-12-20
  7 in total

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