| Literature DB >> 2705486 |
S Shen-Schwarz1, L M Hill, U Surti, S Marchese.
Abstract
We present the necropsy findings of a 21-week-gestation male fetus with deletion of the terminal portion of long arm of chromosome 6 [46,XY,del(6)(q23----qter)]. Major anomalies include intrauterine growth retardation, facial anomalies, nuchal cyst, scoliosis, bilateral diaphragmatic hernias, persistent common atrioventricular canal, absent olfactory bulbs and agenesis of corpus callosum. In aberrations of chromosome 6q, patients usually have psychomotor retardation, somatic growth failure, and facial anomalies; nuchal cyst and bilateral diaphragmatic hernias have not yet been described.Entities:
Mesh:
Year: 1989 PMID: 2705486 DOI: 10.1002/ajmg.1320320117
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299