Preimplantation genetic diagnosis: present and future.

Authors: Fragouli, E.

Journal: J Assist Reprod Genet

Volume: 24

Issue: 6

Pages: 201-207

ISSN: 1058-0468

DOI: 10.1007/s10815-007-9112-2

Abstract:

PURPOSE: Preimplantation genetic diagnosis (PGD) was developed more than a decade ago and aims to identify embryos free of genetic disease attributed either to gene mutations or chromosome errors. The purpose of this article is to provide an update on the current status and future prospects of PGD. METHODS: Review of studies employing different strategies for the detection of single gene defects, and chromosome abnormalities, both structural and numerical in the context of PGD. RESULTS: Amplification of several DNA fragments is feasible via multiplex PCR for the PGD of single gene disorders, whilst current FISH protocols employ up to 10 probes to identify embryos with a normal chromosome complement. New methods are being developed which will enable the assessment of the entire chromosome complement of embryonic blastomeres. CONCLUSIONS: PGD has come a long way since its first application, and has become very accurate and reliable. Technical advances in the field of preimplantation genetics mean that PGD holds great promise for the future.

Source: PubMed

Preimplantation genetic diagnosis: present and future

Authors: Fragouli, E.

Journal: JOURNAL OF ASSISTED REPRODUCTION AND GENETICS

Volume: 24

Issue: 6

Pages: 201-207

eISSN: 1573-7330

ISSN: 1058-0468

DOI: 10.1007/s10815-007-9112-2

Source: Web of Science (Lite)

Preimplantation genetic diagnosis: present and future.

Authors: Fragouli, E.

Journal: Journal of assisted reproduction and genetics

Volume: 24

Issue: 6

Pages: 201-207

eISSN: 1573-7330

ISSN: 1058-0468

DOI: 10.1007/s10815-007-9112-2

Abstract:

Purpose

Preimplantation genetic diagnosis (PGD) was developed more than a decade ago and aims to identify embryos free of genetic disease attributed either to gene mutations or chromosome errors. The purpose of this article is to provide an update on the current status and future prospects of PGD.

Methods

Review of studies employing different strategies for the detection of single gene defects, and chromosome abnormalities, both structural and numerical in the context of PGD.

Results

Amplification of several DNA fragments is feasible via multiplex PCR for the PGD of single gene disorders, whilst current FISH protocols employ up to 10 probes to identify embryos with a normal chromosome complement. New methods are being developed which will enable the assessment of the entire chromosome complement of embryonic blastomeres.

Conclusions

PGD has come a long way since its first application, and has become very accurate and reliable. Technical advances in the field of preimplantation genetics mean that PGD holds great promise for the future.

Source: Europe PubMed Central