Literature DB >> 19638686

Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation.

F Tinsa1, Y Chebbi, M Meddeb, D Bousnina, K Boussetta, S Bousnina.   

Abstract

A male infant with partial monosomy 10 q and partial trisomy 11q as a result of de novo unbalanced translocation between the long arms of chromosomes 10 and 11: der(10)t(10;11)(q26;q13) is described. He had craniofacial dysmorphy, congenital heart defects, urogenital and cerebral anomalies, and severe developmental delay. To the best of our knowledge, this is the first report of this combination of chromosomal abnormalities.

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Year:  2009        PMID： 19638686     DOI： 10.1007/BF03195685

Source DB:  PubMed          Journal:  J Appl Genet        ISSN： 1234-1983            Impact factor:   3.240


  10 in total

1.  Partial monosomy 10q with partial trisomy 11q due to paternal balanced translocation.

Authors:  K Maruyama; T Koizumi; H Ikeda
Journal:  J Paediatr Child Health       Date:  2001-04       Impact factor: 1.954

Review 2.  Terminal deletion of chromosome 10q: clinical features and literature review.

Authors:  S Tanabe; T Akiba; M Katoh; T Satoh
Journal:  Pediatr Int       Date:  1999-10       Impact factor: 1.524

3.  Terminal deletion of chromosome 10q and its clinical features.

Authors:  R Kogasaka; T Morohoshi; Y Sawada; M Fujiwara
Journal:  Acta Paediatr Jpn       Date:  1990-02

4.  Deletions of the long arm of chromosome 10.

Authors:  S D Shapiro; K L Hansen; L M Pasztor; J H DiLiberti; R J Jorgenson; R S Young; C M Moore
Journal:  Am J Med Genet       Date:  1985-01

5.  Monosomy 10qter due to a balanced familial translocation: t(10;16)(q25.2;q24).

Authors:  R D Wegner; J Kunze; H Paust
Journal:  Clin Genet       Date:  1981-02       Impact factor: 4.438

Review 6.  Partial monosomy of distal 10q: three new cases and a review.

Authors:  D J Waggoner; C K Chow; S B Dowton; M S Watson
Journal:  Am J Med Genet       Date:  1999-09-03

7.  Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26).

Authors:  T Tsukuda; I Nagata; H Sawada; J Murakami; K Hanaki; H Urashima; T Kaneda; N Shimizu; N Kaibara; N Kodama; T Ohzeki; K Shiraki
Journal:  Clin Genet       Date:  1996-10       Impact factor: 4.438

8.  Partial trisomy 11q due to paternal t(11q;18p); further delineation of the clinical picture.

Authors:  H F de France; F A Beemer; R C Senders; L J Gerards; B P Cats
Journal:  Clin Genet       Date:  1984-03       Impact factor: 4.438

9.  Partial 11q trisomy syndrome.

Authors:  H Pihko; E Therman; I A Uchida
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 10.  Terminal deletion of the long arm of chromosome 10.

Authors:  S Scigliano; M J Grégoire; M Schmitt; P H Jonveaux; B LeHeup
Journal:  Clin Genet       Date:  2004-04       Impact factor: 4.438
  10 in total
  2 in total

1.  Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2).

Authors:  Alina Teresa Midro; Barbara Panasiuk; Beata Stasiewicz-Jarocka; Marta Olszewska; Ewa Wiland; Marta Myśliwiec; Maciej Kurpisz; Lisa G Shaffer; Marzena Gajecka
Journal:  J Hum Genet       Date:  2014-10-16       Impact factor: 3.172

2.  Clinical and molecular evaluations of siblings with "pure" 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3).

Authors:  Rongyu Chen; Chuan Li; Bobo Xie; Jin Wang; Xin Fan; Jingsi Luo; Xuyun Hu; Shaoke Chen; Yiping Shen
Journal:  Mol Cytogenet       Date:  2014-12-24       Impact factor: 2.009
  2 in total

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