Diagnóstico Prenatal II: importancia de los marcadores ecográficos en el diagnóstico prenatal de cromosomopatías.

Translated title of the contribution: Prenatal diagnosis. II. Importance of ultrasonographic markers in prenatal diagnosis of chromosome abnormalities

M. Prieto-Carrasquero, A. Molero, N. Carrasquero, A. Del Villar, S. González-Ferrer, A. Rojas, J. Brito, R. Mena, L. González, F. Pérez, F. Alvarez, M. Quintero, W. Fulcado

Research output: Contribution to journalArticle

2 Scopus citations


The Medical Genetic Unit of the University of Zulia (MGUUZ) has developed a Prenatal Diagnosis Program (PDP) since January-1993, in which Genetic Risk Factors are determined in couples who request prenatal genetic counseling. In this program, different prenatal diagnostic procedures are performed to detect congenital defects during intrauterine life. One of these procedures is the Fetal Sonogram (FS). FS is a non invasive technique which permits the prenatal diagnosis of many genetic dysmorphic syndromes. Through the search of abnormal specific characteristics in the fetus, chromosomopathies may be suspected. These findings are named "Echosonographic Markers of Chromosomal Abnormalities" (EMCA). During three years (January-1993 to December-1996), patients attended in the PDP included 321 pregnant women in which 312 FS were performed. Abnormal outcomes were 22 (17 with isolated congenital malformations and 5 with EMCA). Only one fetus with chromosome abnormality (46,XX21q-) could not be detected by FS. The goals of this paper are: 1) to report 5 patients with sonographic markers suggestive of chromosomal abnormalities and 2) to show the FS usefulness in prenatal diagnosis of chromosompathies. We conclude that, in the search of the EMCA the FS should be offered systematically to all pregnant women without recognizable genetic risk. They are the main group with optimal reproductive age and in consequence, with the possibility of having a relatively major number of conception outcomes with congenital defects, with or without chromosomic etiology. The majority of those defects can be detected by FS and could allow us to select the patients in which the use of an invasive prenatal diagnostic procedure could be justified.

Original languageSpanish
Pages (from-to)257-272
Number of pages16
JournalInvestigación clínica
Issue number4
Publication statusPublished - Dec 1998
Externally publishedYes


ASJC Scopus subject areas

  • Medicine(all)

Cite this

Prieto-Carrasquero, M., Molero, A., Carrasquero, N., Del Villar, A., González-Ferrer, S., Rojas, A., ... Fulcado, W. (1998). Diagnóstico Prenatal II: importancia de los marcadores ecográficos en el diagnóstico prenatal de cromosomopatías. Investigación clínica, 39(4), 257-272.