| Literature DB >> 15849798 |
F Vialard1, R Robyr, Y Hillion, D Molina Gomes, J Selva, Y Ville.
Abstract
5p deletion syndrome commonly known as cri du chat is well described in affected neonates with catlike cry and hypotonia. Karyotyping will usually show a deletion of the short arm of one chromosome 5 with variable breakpoints. Only a few cases have been reported prenatally, and the fetal form of the syndrome has not been clearly individualised. We report a new case of 5p deletion syndrome diagnosed prenatally in association with Dandy-Walker syndrome and agenesis of the corpus callosum. Other brain anomalies have been reported previously, but this unusual association suggests the use of a specific probe in the investigation of these malformations.Entities:
Mesh:
Year: 2005 PMID: 15849798 DOI: 10.1002/pd.1130
Source DB: PubMed Journal: Prenat Diagn ISSN: 0197-3851 Impact factor: 3.050