SHORT-RIB POLYDACTYLY SYNDROME (SRPS) TYPE-III DIAGNOSED DURING ROUTINE PRENATAL ULTRASONOGRAPHIC SCREENING - A CASE-REPORT

Citation
I. Meizner et Y. Barnhard, SHORT-RIB POLYDACTYLY SYNDROME (SRPS) TYPE-III DIAGNOSED DURING ROUTINE PRENATAL ULTRASONOGRAPHIC SCREENING - A CASE-REPORT, Prenatal diagnosis, 15(7), 1995, pp. 665-668
Citations number
8
Categorie Soggetti
Obsetric & Gynecology
Journal title
ISSN journal
01973851
Volume
15
Issue
7
Year of publication
1995
Pages
665 - 668
Database
ISI
SICI code
0197-3851(1995)15:7<665:SPS(TD>2.0.ZU;2-3
Abstract
The prenatal diagnosis of skeletal dysplasias is often initiated by th e finding of a shortened extremity during a routine sonographic examin ation. Second-trimester diagnosis of these anomalies allows the couple to consider the option of terminating a pregnancy when a lethal anoma ly is detected, A 21-year-old Bedouin woman underwent routine ultrason ographic screening at 20 weeks' gestation. Severe micromelia, a narrow thorax with shortened ribs, and postaxial polydactyly were detected. The patient delivered a male dwarf at 20 weeks' gestation following pr ostaglandin induction of labour for a diagnosis of short-rib polydacty ly syndrome type III. The prenatal ultrasonographic diagnosis of short -rib polydactyly syndrome type III was made at 20 weeks' gestation, al lowing termination of the pregnancy. A proper sonographic approach to skeletal dysplasias allows both early detection and differentiation be tween lethal and non-lethal anomalies.