Literature DB >> 29666354

Double trisomy (XXX+21 karyotype) in a six-year-old girl with down phenotype.

Laura Daniela Vergara-Mendez1, Claudia Talero-Gutiérrez, Alberto Velez-Van-Meerbeke.   

Abstract

We describe a case of a six-year-old girl who presents multiple dysmorphic features characteristic of Down's syndrome. She has a significant general developmental delay, with a score that correspond to 32 months of developmental age. This delay is especially in language, with a very scant vocabulary. She communicates with some hand sign words or pointing, although her auditory responses in hearing test were normal. Two previous karyotype studies showed 47, XXX, +21 anomalies. This double trisomy is a rare condition described in isolated cases in the literature and none of these refers to the developmental aspects of these children (Balwan et al. 2008; Li et al. 2004; Park et al. 1995; Day et al. 1963).

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Year:  2018        PMID: 29666354

Source DB:  PubMed          Journal:  J Genet        ISSN: 0022-1333            Impact factor:   1.166


  11 in total

1.  Double trisomy.

Authors:  Shibo Li; Susan Hassed; John J Mulvihill; Ambika K Nair; Deborah J Hopcus
Journal:  Am J Med Genet A       Date:  2004-01-01       Impact factor: 2.802

Review 2.  Double trisomy (48,XXY,+21) in monozygotic twins: case report and review of the literature.

Authors:  Dimitrios Iliopoulos; George Poultsides; Vasiliki Peristeri; Georgia Kouri; Alexandros Andreou; Nikolaos Voyiatzis
Journal:  Ann Genet       Date:  2004 Jan-Mar

3.  Cytogenetic analysis of 1572 cases of Down syndrome: a report of double aneuploidy and novel findings 47,XY, t(14;21)(q13;q22.3)mat,+21 and 45,XX,t(14;21) in an Indian population.

Authors:  Swarna Mandava; Neeraja Koppaka; Vinay Bhatia; Bibhu Ranjan Das
Journal:  Genet Test Mol Biomarkers       Date:  2010-08

4.  Cytogenetic profile in 1,921 cases of trisomy 21 syndrome.

Authors:  Francisco Flores-Ramírez; Claudia Palacios-Guerrero; Constanza García-Delgado; Ariadna Berenice Morales-Jiménez; Christian Martín Arias-Villegas; Alicia Cervantes; Verónica Fabiola Morán-Barroso
Journal:  Arch Med Res       Date:  2015-08-24       Impact factor: 2.235

Review 5.  Epidemiology of double aneuploidies involving chromosome 21 and the sex chromosomes.

Authors:  Natalia V Kovaleva; David E Mutton
Journal:  Am J Med Genet A       Date:  2005-04-01       Impact factor: 2.802

6.  Double trisomy with 48, XXX+21 karyotype in a Down's syndrome child from Jammu and Kashmir, India.

Authors:  Wahied Khawar Balwan; Parvinder Kumar; T R Raina; Subash Gupta
Journal:  J Genet       Date:  2008-12       Impact factor: 1.166

7.  Double trisomy in spontaneous miscarriages: cytogenetic and molecular approach.

Authors:  Dan Diego-Alvarez; Carmen Ramos-Corrales; Maria Garcia-Hoyos; Ana Bustamante-Aragones; Diego Cantalapiedra; Joaquin Diaz-Recasens; Elena Vallespin-Garcia; Carmen Ayuso; Isabel Lorda-Sanchez
Journal:  Hum Reprod       Date:  2005-12-16       Impact factor: 6.918

8.  Double trisomy revisited--a multicenter experience.

Authors:  Mark Micale; Janet Insko; Salah A D Ebrahim; Adewale Adeyinka; Cassandra Runke; Daniel L Van Dyke
Journal:  Prenat Diagn       Date:  2010-02       Impact factor: 3.050

Review 9.  Triple X syndrome: a review of the literature.

Authors:  Maarten Otter; Constance T R M Schrander-Stumpel; Leopold M G Curfs
Journal:  Eur J Hum Genet       Date:  2009-07-01       Impact factor: 4.246

10.  Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21.

Authors:  V M Park; R R Bravo; L P Shulman
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

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  1 in total

1.  A rare case of NIPT discrepancy caused by the placental mosaicism of three different karyotypes, 47,XXX, 47,XX,+21, and 48,XXX,+21.

Authors:  Jin Li; Mingshui Xie; Fang Wang; Jianhong Ma; Jiafu Li; Chen Chen; Zhimin Li; Juan Wang; Yuanzhen Zhang; Yirong Li
Journal:  Mol Genet Genomic Med       Date:  2020-05-28       Impact factor: 2.183

  1 in total

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