BetaThis search tool is in development. Find out more.
Digital Images

Patau's syndrome karyotype 47,XY,+13

Wessex Reg. Genetics Centre

Available online

view Patau's syndrome karyotype 47,XY,+13
View

License

Attribution 4.0 International (CC BY 4.0)

You can use this work for any purpose, including commercial uses, without restriction under copyright law. You should also provide attribution to the original work, source and licence.

Creative Commons Attribution (CC BY 4.0) terms and conditions https://creativecommons.org/licenses/by/4.0

Credit: Patau's syndrome karyotype 47,XY,+13. Credit: Wessex Reg. Genetics Centre. Attribution 4.0 International (CC BY 4.0)


About this work

Description

Trisomy 13 syndrome (formerly Patau's syndrome), 47,XY,+13. This male has a full complement of chromosome, plus an extra chromosome 13. Symptoms of this severe syndrome include microcephaly, cleft lip or palate, polydactyly, and flexion deformities of the fingers. Infants are deaf and blind and rarely survive more than a few weeks or months. The syndrome is associated with advanced maternal age.



Identifiers


We’re improving the information on this page. Find out more.