Patau Syndrome: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
Patau Syndrome is a [[Trisomy|trisomy]] of chromosome 13 due to a [[ | Patau Syndrome is a [[Trisomy|trisomy]] of [[chromosome 13|chromosome 13]] due to a [[Nondisjuction|nondisjunction]] during [[Meiosis|meiosis]]. Patau Syndrome can also result from a [[Translocation|Robersonian translocation]], a section of chromosome 13 attacthes to another [[Chromosome|chromosome]]. This results in [[Cell|cell]] containing 2 intact copies of chromosome 13 and an extra partial copy. Patau Syndrome has a prevalence of around 1 in every 10,000 live births<ref>"http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002625/", Trisomy 13, PubMed Health, 04-08-2011. Retrieved 17-10-2012.</ref> . | ||
=== References<br> === | |||
<br> | |||
<references /><br> | <references /><br> | ||
Revision as of 16:09, 17 October 2012
Patau Syndrome is a trisomy of chromosome 13 due to a nondisjunction during meiosis. Patau Syndrome can also result from a Robersonian translocation, a section of chromosome 13 attacthes to another chromosome. This results in cell containing 2 intact copies of chromosome 13 and an extra partial copy. Patau Syndrome has a prevalence of around 1 in every 10,000 live births[1] .
References
- ↑ "http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002625/", Trisomy 13, PubMed Health, 04-08-2011. Retrieved 17-10-2012.