| Literature DB >> 4025391 |
F Razavi-Encha, O Raoul, M C Lescs, C Danan.
Abstract
We report on a case of dup(18q) due to de novo translocation 46,XX,-21,t(18;21)(18qter----cen----21qter). The patient had many characteristic signs of full trisomy 18 except for internal organ malformations and early death. We review the phenotype-karyotype correlations between full trisomy 18 and dup(18q) and discuss the possibility of the existence of "critical zone(s)" at the proximal or/and distal region of 18q responsible for most signs of trisomy 18, such as congenital heart defect and early death.Entities:
Mesh:
Year: 1985 PMID: 4025391 DOI: 10.1002/ajmg.1320210321
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299