Literature DB >> 2935479

Trisomy 21 Down syndrome. II. Structural chromosome rearrangements in the parents.

I A Uchida, V C Freeman.   

Abstract

In a series of 374 families with Down syndrome progeny, structural chromosome rearrangements were detected in the parents of six children with regular trisomy. The aberrations were reciprocal translocations and inversions. In all three informative families, the parent who transmitted the extra chromosome was not the one with the structural rearrangement. Among the three non-informative families there was one in which both parents carried different reciprocal translocations. In two other families a chromosome aberration was detected: a triple X mother and a father with a Philadelphia chromosome. Omitting the four parents with possible biased ascertainment, 0.4% had a chromosome rearrangement. When the parents with constitutional chromosome aberrations and those with mosaicism, described previously, are combined, the frequency of chromosomally abnormal parents lies between 1.9% and 3.2%. When correlated with parental transmission of the extra chromosome, mosaicism rather than structural rearrangements appears to be of etiologic significance.

Entities:  

Mesh:

Year:  1986        PMID: 2935479     DOI: 10.1007/bf00283928

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  10 in total

1.  Inherited t2q-/15q+ translocation and Down's syndrome.

Authors:  C Stoll; J J Kuss; E Schneegans
Journal:  Clin Genet       Date:  1976-01       Impact factor: 4.438

2.  A PATIENT WITH TRISOMY 21 AND A RECIPROCAL TRANSLOCATION IN THE 13-15 GROUP.

Authors:  L ZERGOLLERN; D HOEFNAGEL; K BENIRSCHKE; P A CORCORAN
Journal:  Cytogenetics       Date:  1964

3.  A D/F TRANSLOCATION IN A CASE OF REGULAR TRISOMY 21 DOWN'S SYNDROME.

Authors:  U GRIPENBERG; E AIRAKSINEN
Journal:  Cytogenetics       Date:  1964

4.  A FAMILY SHOWING TRANSMISSION OF A D/D RECIPROCAL TRANSLOCATION AND A CASE OF REGULAR 21-TRISOMIC DOWN'S SYNDROME.

Authors:  J L HAMERTON; F GIANNELLI; C O CARTER
Journal:  Cytogenetics       Date:  1963

Review 5.  AUTOSOMAL DISORDERS.

Authors:  J LEJEUNE
Journal:  Pediatrics       Date:  1963-09       Impact factor: 7.124

6.  A new hypothesis on the nature and sequence of meiotic events in the female of Drosophila melanogaster.

Authors:  R F GRELL
Journal:  Proc Natl Acad Sci U S A       Date:  1962-02       Impact factor: 11.205

7.  Association of D/D translocations with fetal wastage and aneuploidy. A report of four families.

Authors:  P M Fernhoff; D N Singh; J Hanson; S Trusler; C R Dumont; A T Chen
Journal:  J Med Genet       Date:  1976-10       Impact factor: 6.318

8.  A familial, balanced 2-5 translocation associated with trisomy 21 in one individual.

Authors:  C Lundsteen; S Vestermark; J Philip
Journal:  Hum Hered       Date:  1974       Impact factor: 0.444

9.  Trisomy 9p syndrome and XYY syndrome in siblings.

Authors:  K H Gustavson; J Wahlström
Journal:  Clin Genet       Date:  1977-01       Impact factor: 4.438

10.  Trisomy 21 Down syndrome. Parental mosaicism.

Authors:  I A Uchida; V C Freeman
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

  10 in total
  3 in total

1.  Triploidy arising from a first meiotic non-disjunction in a mother carrying a reciprocal translocation.

Authors:  L Rochon; M J Vekemans
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

2.  Chromosome analysis by spectral karyotyping of spermatozoa from an oligoasthenozoospermic carrier of a 10; 21 reciprocal translocation.

Authors:  Mitsuhiro Motoyama; Kazumasa Takahashi; Shuichi Ogawa; Michiko Ohno; Midori Yoshizawa; Emiko Fukui; Shigeo Araki
Journal:  Hum Cell       Date:  2011-10-12       Impact factor: 4.174

3.  De novo microdeletion on an inherited Robertsonian translocation chromosome: a cause for dysmorphism in the apparently balanced translocation carrier.

Authors:  D T Bonthron; S J Smith; J Fantes; C M Gosden
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.