| Literature DB >> 17668239 |
Altuğ Koç1, Derya Kan, Kadri Karaer, Mehmet A Ergün, Meral Yirmibeş Karaoğuz, Kivilcim Gücüyener, Sophie Hinreiner, Thomas Liehr, E Ferda Perçin.
Abstract
Major neurological disorders may accompany rare chromosomal abnormalities. As an example of this rare condition, we present a case with microcephaly, mental retardation, developmental delay, hyperactivity, stereotypic movements, seizures and dysmorphic facial appearance in whom a mosaic ring chromosome 18 was found [45,XX,-18/46,XX,r(18)/46,XX,dicr(18)]. Although ring chromosome 18 phenotype has been known for a long time, this is the third reported patient with a dicentric ring chromosome 18 mosaicism. The presented case will contribute to the identification of the genotype-phenotype correlation in chromosome 18 anomalies.Entities:
Mesh:
Year: 2007 PMID: 17668239 DOI: 10.1007/s00431-007-0568-y
Source DB: PubMed Journal: Eur J Pediatr ISSN: 0340-6199 Impact factor: 3.183