Literature DB >> 10440828

Partial duplication of 4q12q13 leads to a mild phenotype.

V Shashi1, M N Berry, C Santos, M J Pettenati.   

Abstract

We report on the second case of duplication (4)(q12q13) with microcephaly, mental retardation, and minor facial anomalies. Duplications involving the distal region of chromosome 4q are well described and share common clinical findings. However, phenotypic abnormalities of duplications of the proximal portion of chromosome 4q are relatively unknown. A comparison of the clinical manifestations of our patient and the single published case suggests that the phenotype of this proximal 4q duplication is relatively mild. This study emphasizes the need to perform chromosome analysis in similar mildly affected/nonspecific cases. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10440828

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

1.  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

2.  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

3.  Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report.

Authors:  Reza Mohammadi; Raheleh Taheri; Fatemeh Shahriyari; Farnaz Feiz; Zahra Mohammadi; Sadegh Shirian; Reza Raoofian; Abdorrasoul Malekpour; Reza Pazhoomand
Journal:  Int J Reprod Biomed       Date:  2021-06-23

Review 4.  A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature.

Authors:  Roxana Popescu; Mihaela Grămescu; Lavinia Caba; Monica-Cristina Pânzaru; Lăcrămioara Butnariu; Elena Braha; Setalia Popa; Cristina Rusu; Georgeta Cardos; Monica Zeleniuc; Violeta Martiniuc; Cristina Gug; Luminiţa Păduraru; Maria Stamatin; Carmen C Diaconu; Eusebiu Vlad Gorduza
Journal:  Genes (Basel)       Date:  2021-12-07       Impact factor: 4.096

  4 in total

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