File:Trisomy 13 polydactyly.jpg
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Trisomy 13 Polydactyly
A 37 2/7 week gestational age male infant with Patau syndrome demonstrating hand 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
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
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 21:53, 6 May 2012 | | 596 × 543 (56 KB) | Z8600021 (talk | contribs) | ==Trisomy 13 Polydactyly== A 37 2/7 week gestational age male infant with Patau syndrome demonstrating hand polydactyly. Trisomy 13 (Patau syndrome) is a rare (1 in 10,000 newborns) developmental genetic abnormality (aneuploidy) with three copies of chr |
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