NDLI: Preimplantation diagnosis of genetic diseases.

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Year: 2010 Volume: 56 Issue: 3

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Preimplantation diagnosis of genetic diseases.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Adiga, S. K. Kalthur, G. Kumar, P. Girisha, K. M.
Description	Country affiliation: India Author Affiliation: Adiga SK ( Division of Reproductive Medicine, Kasturba Medical College, Manipal University, Manipal, India.)
Abstract	One of the landmarks in clinical genetics is prenatal diagnosis of genetic disorders. The recent advances in the field have made it possible to diagnose the genetic conditions in the embryos before implantation in a setting of in vitro fertilization. Polymerase chain reaction and fluorescence in situ hybridization are the two common techniques employed on a single or two cells obtained via embryo biopsy. The couple who seek in vitro fertilization may screen their embryos for aneuploidy and the couple at risk for a monogenic disorder but averse to abortion of the affected fetuses after prenatal diagnosis, are likely to be the best candidates to undergo this procedure. This article reviews the technique, indications, benefits, and limitations of pre-implantation genetic testing in clinical practice.
File Format	HTM / HTML
ISSN	00223859
e-ISSN	09722823
Journal	Journal of Postgraduate Medicine
Issue Number	4
Volume Number	56
Language	English
Publisher	MedKnow Publication
Publisher Date	2010-10-01
Publisher Place	India
Access Restriction	Open
Subject Keyword	Discipline Medicine Embryo Implantation Genetics Genetic Diseases, Inborn Diagnosis Preimplantation Diagnosis Prenatal Diagnosis Biopsy Chromosome Aberrations Genetic Testing In Situ Hybridization, Fluorescence Polymerase Chain Reaction Pregnancy
Content Type	Text
Resource Type	Article
Subject	Medicine

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Similar Documents

Progress in preimplantation genetics.

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