학술논문

Prenatal diagnosis of 18q-syndrome: a case of fetal mosaicism with a normal karyotype in chorionic villi.
Document Type
Academic Journal
Source
Fetal Diagnosis & Therapy (FETAL DIAGN THER), 2010; 28(3): 180-185. (6p)
Subject
Language
English
ISSN
1015-3837
Abstract
We report a case of fetoplacental discrepancy with normal karyotype on chorionic villi and deletion of the long arm of chromosome 18 on amniotic fluid. Cytogenetic tests were repeated because of a short corpus callosum on ultrasound examination. This 18q-syndrome has been reported to be associated with poor neurodevelopmental outcome.