Prenatal diagnostic tests of genetic disorders: review article

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

ARYAN ZAHRA; BAHADORI Atekeh; D.FARHUD DARIUSH

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ) Year:2019 | Volume:77 | Issue:1 Page(s): 8-12

Download Full-Text

Persian Verion

View:

1,648

Download:

Cites:

Information Journal Paper

Title

Prenatal diagnostic tests of genetic disorders: review article

Author(s)

ARYAN ZAHRA | BAHADORI Atekeh | D.FARHUD DARIUSH | Issue Writer Certificate

Keywords

diagnostic testsQ1

genetic diseasesQ2

prenatal diagnosisQ2

screening testsQ1

Abstract

The purpose of prenatal diagnosis tests is insisting of diagnosis of neonatal disorders, preparing a range of informed choices and making couples at risk to be ready for having children with genetic disorders as well. The aim of this article is to investigate all of the tests in order to determine the best one which has the lowest risk and the highest sensitivity. screening tests (maternal blood test and ultrasonography for first and second trimester) are testing patients without symptoms who are at low risk. These tests are carried out in the early stages of pregnancy, and the risk of genetic diseases would be estimated. They are safe and also might be helpful in determining whether invasive prenatal genetic tests including chorionic villus sampling, amniocentesis, and percutaneous umbilical blood sampling are needed. Diagnostic test is insisting of invasive tests: amniocentesis, chorionic villus sampling (CVS), cordocentesis, and preimplantation genetic diagnosis (PGD), which is a genetic test on cells removed from embryos to help select the best ones to avoid some of genetic diseases, fluorescence in situ hybridization (FISH), QF-PCR, multiplex ligation probe amplification (MLPA), next generation sequencing (NGS), comparative genomic hybridization (CGH), and non-invasive tests: ultrasound, prenatal sonography, cell free fetal DNA, triple and quadruple screen: alpha fetoprotein (AFP), human chorionic gonadotropin (hCG), unconjugated estriol (uE3), inhibin-A)...

Cites

No record.

References

No record.

Cite

APA: Copy

ARYAN, ZAHRA, BAHADORI, Atekeh, & D.FARHUD, DARIUSH. (2019). Prenatal diagnostic tests of genetic disorders: review article. TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ), 77(1 ), 8-12. SID. https://sid.ir/paper/368978/en

Vancouver: Copy

ARYAN ZAHRA, BAHADORI Atekeh, D.FARHUD DARIUSH. Prenatal diagnostic tests of genetic disorders: review article. TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ)[Internet]. 2019;77(1 ):8-12. Available from: https://sid.ir/paper/368978/en

IEEE: Copy

ZAHRA ARYAN, Atekeh BAHADORI, and DARIUSH D.FARHUD, “Prenatal diagnostic tests of genetic disorders: review article,” TEHRAN UNIVERSITY MEDICAL JOURNAL (TUMJ), vol. 77, no. 1 , pp. 8–12, 2019, [Online]. Available: https://sid.ir/paper/368978/en

Related Journal Papers