Pregnancy outcome of a case  with a rare chromosomal balanced  translocation 46XX t(4;13)

Yaliwal, Laxmi V.; Desai, Rathnamala M.; Sunil Kumar, K. S.

dc.contributor.author	Yaliwal, Laxmi V.
dc.contributor.author	Desai, Rathnamala M.
dc.contributor.author	Sunil Kumar, K. S.
dc.date.accessioned	2015-07-28T20:58:12Z
dc.date.available	2015-07-28T20:58:12Z
dc.date.issued	2012-05
dc.identifier.citation	Journal of Clinical and Diagnostic Research. 2012 May; 6(4 Suppl-2): 736-737.	en_US
dc.identifier.issn	0973-709X, 2249-782X
dc.identifier.uri	http://hdl.handle.net/123456789/677
dc.description.abstract	Chromosomal translocations are rare. The unbalanced trans- locations may lead to structural malformations. The balanced translocations may not result in phenotypic alterations, as there is no loss or gain of genetic material. We are reporting here, a case of a balanced translocation carrier 46XX t(4;13) and her pregnancy outcome. Ultrasound at 11-12 weeks of gestation for determining the nuchal translucency thickness and for prenatal genetic testing might be considered as a part of the investiga- tions for pregnancies with a parental balanced chromosomal translocation.	en_US
dc.language.iso	en	en_US
dc.publisher	JCDR Research and Publications (Pvt) Limited	en_US
dc.subject	Chromosomal translocation	en_US
dc.subject	Duplication 4q/ Pregnancy complications	en_US
dc.title	Pregnancy outcome of a case with a rare chromosomal balanced translocation 46XX t(4;13)	en_US
dc.type	Article	en_US