Literature DB >> 3300332

Partial duplication 8q12----q21.2 in two sibs with maternally derived insertional and reciprocal translocations: case reports and review of partial duplications of chromosome 8.

A P Walker, M Bocian.   

Abstract

We report on two sibs with duplication of the segment 8q12----8q21.2 resulting from malsegregation of a maternal insertional translocation: [inv ins (5;8)(p13;q12q21.2)]. The mother also carries a reciprocal translocation [t(1;6)(q31;q5)], which was transmitted in the balanced state to the propositi and to a phenotypically normal son and daughter. The literature on two translocations occurring in one individual and on insertional rearrangements is reviewed in terms of reproductive risks to balanced carriers. The two affected infants have a previously undescribed partial duplication of an interstitial segment of 8q and a pattern of abnormalities distinct from those seen in other partial duplications of 8. These infants are reviewed with 78 other cases of partial duplications of chromosome 8 with regard to phenotype-karyotype correlations.

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Year:  1987        PMID: 3300332     DOI: 10.1002/ajmg.1320270103

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

1.  An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito.

Authors:  B H Eussen; G Bartalini; L Bakker; P Balestri; C Di Lucca; J O Van Hemel; H Dauwerse; A M van Den Ouweland; C Ris-Stalpers; S Verhoef; D J Halley; A Fois
Journal:  J Med Genet       Date:  2000-04       Impact factor: 6.318

2.  Partial trisomy of distal 8q derived from mother with mosaic 8q23.3----24.13 deletion, and relatively mild expression of trichorhinophalangeal syndrome I.

Authors:  K Naritomi; K Hirayama
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

3.  Familial distal trisomy 8(q24.13----qter).

Authors:  D R Romain; R A Bloxham; L M Columbano-Green; C J Chapman; R G Parfitt; R H Smythe; H Cairney
Journal:  J Med Genet       Date:  1989-02       Impact factor: 6.318

4.  FRAXF in a patient with chromosome 8 duplication.

Authors:  A M Vianna-Morgante; R C Mingroni-Netto; A C Barbosa; P A Otto; C Rosenberg
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

  4 in total

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