Literature DB >> 1084124

Trisomy iop.

E Yunis, R Silva, A Giraldo.   

Abstract

A stillborn male fetus having a trisomy of the short arm of chromosome No 10 is described. The father is a carrier of the reciprocal translocation 46XY,t(10;21) (10pter leads to 10p11::21p11 leads to 21qter). The clinical picture included growth retardation, bilateral cleft lip and palate, micrognathia, short neck, microphalus and bilateral clubbed feet. The long bones were markedly thinned with spontaneous fractures. Autopsy findings included pulmonary hypoplasia and renal dysplasia. Previous reports of trisomy 10 and trisomy of the short arm of chromosome 10 are discussed.

Entities:  

Mesh:

Year:  1976        PMID: 1084124

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


  11 in total

1.  Risk for short arm 10 trisomy. A segregation analysis of eleven families with different translocations.

Authors:  J Stene; S Stengel-Rutkowski
Journal:  Hum Genet       Date:  1977-11-02       Impact factor: 4.132

2.  New chromosomal dysmorphic syndromes. 2. Trisomy 10p.

Authors:  S Stengel-Rutkowski; J D Murken; R Frankenberger; M Riechert; H Spiess; A Rodewald; J Stene
Journal:  Eur J Pediatr       Date:  1977-10-12       Impact factor: 3.183

Review 3.  Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

Authors:  P Jalbert; B Sele
Journal:  J Med Genet       Date:  1979-12       Impact factor: 6.318

4.  Partial trisomy 10p in two generations.

Authors:  I W Lurie; G I Lazjuk; D B Gurevich; G I Kravtzoa; M K Nedzved; I A Shved
Journal:  Hum Genet       Date:  1978-03-17       Impact factor: 4.132

5.  Brother and sister with trisomy 10p. 46,XY,(22p+)mat; 46,XX,(22p+)mat.

Authors:  P de Chieri; E Spatuzza; J M Bonich
Journal:  Hum Genet       Date:  1978-11-24       Impact factor: 4.132

6.  Reciprocal translocations: a way to predict the mode of imbalanced segregation by pachytene-diagram drawing.

Authors:  P Jalbert; B Sele; H Jalbert
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

7.  Familial translocation t(10;21)(q22;q22).

Authors:  A Delicado; I L Pajares; P Vicente; F Hawkins
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

Review 8.  Genetic factors in congenital diaphragmatic hernia.

Authors:  A M Holder; M Klaassens; D Tibboel; A de Klein; B Lee; D A Scott
Journal:  Am J Hum Genet       Date:  2007-04-04       Impact factor: 11.025

9.  Duplication deficiency as the result of meiotic segregation of a maternal InV (10).

Authors:  E Yunis; O Torres de Caballero
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

10.  Trisomy 10p due to a de novo t(10p;13p).

Authors:  V Aller; J A Abrisqueta; A Pérez-Castillo; J del Mazo; M A Martín-Lucas; M L de Torres
Journal:  Hum Genet       Date:  1979-01-25       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.