Literature DB >> 2585464

Maternal translocation (9;18) with two abnormal offspring each with different chromosome derivatives.

M Pearson1, C Riske, J E Allanson.   

Abstract

We report a phenotypically normal woman with an apparently balanced reciprocal translocation between chromosomes 9 and 18 [46,XX,t(9;18)(p22;p11.2)], giving rise to unbalanced chromosome complements in two of her children, each of whom received a different derivative chromosome. The proband's karyotype is 46,XY,-18,+der(18), t(9;18)(p22;p11.2)mat, which results in a duplication of the distal portion of the short arm of chromosome 9 with a concomitant deletion of much of the short arm of chromosome 18. The karyotype of the proband's brother is 46, XY,-9,+der(9),t(9;18)(p22;p11.2)mat, which results in a deletion of the distal short arm of chromosome 9 and a duplication of most of the short arm of chromosome 18. The phenotype of each child is significantly different from that of his sib and is not consistent with any previously reported chromosome abnormality.

Entities:  

Mesh:

Year:  1989        PMID: 2585464      PMCID: PMC1015721          DOI: 10.1136/jmg.26.10.655

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  12 in total

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Authors:  O S Alfi; G N Donnell; P W Allderdice; A Derencsenyi
Journal:  Ann Genet       Date:  1976-03

2.  FAMILIAL SHORT ARM DEFICIENCY OF CHROMOSOME 18 CONCOMITANT WITH ARHINENCEPHALY AND ALOPECIA CONGENITA.

Authors:  I A UCHIDA; K N MCRAE; M RAY
Journal:  Am J Hum Genet       Date:  1965-09       Impact factor: 11.025

3.  High resolution of human chromosomes.

Authors:  J J Yunis
Journal:  Science       Date:  1976-03-26       Impact factor: 47.728

4.  The trisomy 9p syndrome.

Authors:  W R Centerwall; J W Beatty-DeSana
Journal:  Pediatrics       Date:  1975-11       Impact factor: 7.124

5.  Type and contretype signs in monosomy and trisomy 9p. On a case 46,XY, del (9) (pter yields p12:).

Authors:  A Hernandez; H Rivera; M Jiménez-Sainz; R Fragoso; Z Nazara; J M Cantu
Journal:  Ann Genet       Date:  1979

6.  Deletion of the short arm of chromosome no.9 (46,9p-): a new deletion syndrome.

Authors:  O Alfi; G N Donnell; B F Crandall; A Derencsenyi; R Menon
Journal:  Ann Genet       Date:  1973-03

7.  Prenatal diagnosis of an inherited translocation between chromosomes No. 9 and 18.

Authors:  A J Ebbin; M G Wilson; J W Towner; J P Slaughter
Journal:  J Med Genet       Date:  1973-03       Impact factor: 6.318

8.  Amniocyte clones for prenatal cytogenetics.

Authors:  F Hecht; D C Peakman; B Kaiser-McCaw; A Robinson
Journal:  Am J Med Genet       Date:  1981

9.  Trisomy 9p with i(9p) and t(9q18p).

Authors:  R Herva; M Koivisto
Journal:  Hum Genet       Date:  1979-09       Impact factor: 4.132

10.  9p Trisomy/18p distal monosomy and multiple cutaneous leiomyomata. Another specific chromosomal site (18pter) in dominantly inherited multiple tumors?

Authors:  J P Fryns; M Haspeslagh; A de Mûelenaere; H van Den Berghe
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

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