File:220px-Patauhand.PNG: Difference between revisions

Latest revision as of 12:35, 4 February 2011

Trisomy 13 Hand

A 37 2/7 week gestational age male infant with Patau syndrome demonstrating polydactyly.

Trisomy 13 (Patau syndrome) is a rare (1 in 10,000 newborns) developmental genetic abnormality (aneuploidy) with three copies of chromosome 13, instead of the usual two copies, there can also be a chromosomal translocation.

Links: Trisomy 13 | Abnormal Development - Genetic

Note - This image was originally uploaded as part of an undergraduate science student project and may contain inaccuracies in either description or acknowledgements. Students have been advised in writing concerning the reuse of content and may accidentally have misunderstood the original terms of use. If image reuse on this non-commercial educational site infringes your existing copyright, please contact the site editor for immediate removal.

Reference

Chan A, Lakshminrusimha S, Heffner R, Gonzalez-Fernandez F.Histogenesis of retinal dysplasia in trisomy 13. Diagn Pathol. 2007 Dec 18;2(1):48 PMID: 18088410 doi:10.1186/1746-1596-2-48

Image source: http://commons.wikimedia.org/wiki/File:Patauhand.PNG

This file is licensed under the Creative Commons Attribution-Share Alike 3.0 Unported, 2.5 Generic, 2.0 Generic and 1.0 Generic license.

File history

Yi efo/eka'e gwa ebo wo le nyangagi wuncin ye kamina wunga tinya nan

	Gwalagizhi	Nyangagi	Dimensions	User	Comment
current	11:15, 16 September 2010		220 × 200 (69 KB)	Z3265772 (talk \| contribs)	This file is licensed under the Creative Commons Attribution-Share Alike 3.0 Unported, 2.5 Generic, 2.0 Generic and 1.0 Generic license. You are free: * to share – to copy, distribute and transmit the work * to remix – to adapt

You cannot overwrite this file.

File usage

The following page uses this file:

2010 Group Project 2

@@ Line 1: / Line 1: @@
+==Trisomy 13 Hand==
+A 37 2/7 week gestational age male infant with Patau syndrome demonstrating polydactyly.
+Trisomy 13 (Patau syndrome) is a rare (1 in 10,000 newborns) developmental genetic abnormality (aneuploidy) with three copies of chromosome 13, instead of the usual two copies, there can also be a chromosomal translocation.
+:'''Links:''' [[Trisomy 13]] | [[Abnormal Development - Genetic]]
+{{Template:Student Image}}
 ==Reference==
+<pubmed>18088410</pubmed>
+Chan A, Lakshminrusimha S, Heffner R, Gonzalez-Fernandez F.Histogenesis of retinal dysplasia in trisomy 13. Diagn Pathol. 2007 Dec 18;2(1):48 PMID: 18088410 doi:10.1186/1746-1596-2-48
 Image source: http://commons.wikimedia.org/wiki/File:Patauhand.PNG
 This file is licensed under the Creative Commons Attribution-Share Alike 3.0 Unported, 2.5 Generic, 2.0 Generic and 1.0 Generic license.
+[[Category:Human]] [[Category:Abnormal Development]] [[Category:Genetic Abnormalities]]