Literature DB >> 6598632

[Duplication of the long arm of chromosome 3 (dup 3q) in a newborn infant whose the father is carrier of pericentric inversion of chromosome 9].

D Ayral, D Raudrant, J P Charleux, B Noel.   

Abstract

The authors report a case of a partial trisomy for the long arm of chromosome 3. The associated morphotypic anomalies are compared with the 31 cases already reported, and allow to further outline a well recognizable morphotype which has similarities with the Brachmann Cornelia de Lange Syndrome. The chromosomal mechanisms which may result in this unbalanced caryotype dup 3 q are discussed, and among them the possible role of a paternal chromosome 9 pericentric inversion, most commonly termed as a normal variant.

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Year:  1984        PMID: 6598632

Source DB:  PubMed          Journal:  Pediatrie        ISSN: 0031-4021


  2 in total

Review 1.  Unique occurrence of Brachmann-de Lange syndrome in a fetus whose mother presented with a diffuse large B-cell lymphoma.

Authors:  Christiane Schiffer; Monika Schiesser; Jutta Lehr; Gholamali Tariverdian; Dieter Glaeser; Heinz Gabriel; Gregor Mikuz; Consolato Sergi
Journal:  Pathol Oncol Res       Date:  2007-10-07       Impact factor: 3.201

2.  Prenatally diagnosed partial trisomy 3q case with an omphalocele and less severe phenotype.

Authors:  Deniz Cemgil Arıkan; Ayhan Coşkun; Ilker Arıkan; Gürkan Kıran; Gülay Ceylaner
Journal:  J Turk Ger Gynecol Assoc       Date:  2010-12-01
  2 in total

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