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World J Radiol. Oct 28, 2013; 5(10): 356-371
Published online Oct 28, 2013. doi: 10.4329/wjr.v5.i10.356
Sonographic markers for early diagnosis of fetal malformations
Maria Daniela Renna, Paola Pisani, Francesco Conversano, Emanuele Perrone, Ernesto Casciaro, Gian Carlo Di Renzo, Marco Di Paola, Antonio Perrone, Sergio Casciaro
Maria Daniela Renna, Paola Pisani, Francesco Conversano, Ernesto Casciaro, Marco Di Paola, Sergio Casciaro, National Council of Research, Institute of Clinical Physiology, c/o Campus Universitario Ecotekne, 73100 Lecce, Italy
Emanuele Perrone, Gian Carlo Di Renzo, Department of Obstetrics and Gynecology, University of Perugia, Santa Maria della Misericordia University Hospital, San Sisto-06132 Perugia, Italy
Antonio Perrone, Obstetrics and Gynecology Department, “Vito Fazzi” Hospital, Piazza Filippo Muratore, 1-73100 Lecce, Italy
Author contributions: All the authors were involved in designing the study and writing the manuscript.
Supported by FESR P.O. Apulia Region 2007-2013-Action 1.2.4 (grant number 3Q5AX31) and the National Council of Research Project AMOLAB
Correspondence to: Sergio Casciaro, PhD, Eng, National Council of Research (IFC-CNR), Institute of Clinical Physiology, c/o Campus Universitario Ecotekne, via per Monteroni, 73100 Lecce, Italy. sergio.casciaro@cnr.it
Telephone: +39-08-32422310 Fax: +39-08-320422341
Received: June 28, 2013
Revised: September 10, 2013
Accepted: September 18, 2013
Published online: October 28, 2013
Abstract

Fetal malformations are very frequent in industrialized countries. Although advanced maternal age may affect pregnancy outcome adversely, 80%-90% of fetal malformations occur in the absence of a specific risk factor for parents. The only effective approach for prenatal screening is currently represented by an ultrasound scan. However, ultrasound methods present two important limitations: the substantial absence of quantitative parameters and the dependence on the sonographer experience. In recent years, together with the improvement in transducer technology, quantitative and objective sonographic markers highly predictive of fetal malformations have been developed. These markers can be detected at early gestation (11-14 wk) and generally are not pathological in themselves but have an increased incidence in abnormal fetuses. Thus, prenatal ultrasonography during the second trimester of gestation provides a “genetic sonogram”, including, for instance, nuchal translucency, short humeral length, echogenic bowel, echogenic intracardiac focus and choroid plexus cyst, that is used to identify morphological features of fetal Down’s syndrome with a potential sensitivity of more than 90%. Other specific and sensitive markers can be seen in the case of cardiac defects and skeletal anomalies. In the future, sonographic markers could limit even more the use of invasive and dangerous techniques of prenatal diagnosis (amniocentesis, etc.).

Keywords: Prenatal diagnosis, Prenatal sonography, Chromosome abnormalities, Nuchal translucency, Fetal echocardiography, Skeletal dysplasia

Core tip: The aim of this paper is to review sonographic markers associated with the most frequent fetal abnormalities (chromosomal anomalies, cardiac defects, skeletal dysplasia) and their sensitivity in prenatal diagnosis. Fetal malformations are very frequent in industrialized countries and the only effective approach for prenatal screening is currently represented by an ultrasound scan. Early detection of abnormalities can optimize pregnancy management and childbirth timing, give the possibility of performing simpler procedures for termination of pregnancy in those patients in whom findings are abnormal, and plan therapeutic treatment of objectively selected diseased fetuses.