Literature DB >> 6982667

8p trisomy in a malformed foetus.

J P Fryns, P Petit, F Moerman, J J Cassiman, H van den Berghe.   

Abstract

A 20-week-old foetus with 8p trisomy, as the unbalanced product of a maternal 7q/8p translocation (karyotype: 46,XX,t(7;8)(q34,p12) is reported. Internal malformations include agenesis of the gall-bladder, left heart hypoplasia and pancreas annulare. Moreover, histologic examination revealed a "neuroblastoma in situ". The possible etiologic relationship between the neuroblastoma and the chromosomal abnormality is briefly discussed.

Entities:  

Mesh：

Year:  1982        PMID： 6982667

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


  4 in total

1.  Trisomy 8p: unusual origin detected by fluorescence in situ hybridization.

Authors:  C M Moore; K Barnum; C I Kaye; K S Kagan-Hallett; J C Liang
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

2.  Germline duplication of chromosome 2p and neuroblastoma.

Authors:  J S Patel; J Pearson; L Willatt; T Andrews; R Beach; A Green
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

3.  Congenital heart disease and neuroblastoma: just coincidence?

Authors:  R Holzer; R C G Franklin
Journal:  Arch Dis Child       Date:  2002-07       Impact factor: 3.791

Review 4.  Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).

Authors:  A S Plomp; J J Engelen; J C Albrechts; C E de Die-Smulders; A J Hamers
Journal:  J Med Genet       Date:  1998-07       Impact factor: 6.318
  4 in total

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