Trisomy 13: Difference between revisions
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Created page with " Trisomy 13 is a genetic condition where the indiviual inhereits an extra copy of chromosome 13. It is also known as patau syndrome ..." |
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Revision as of 20:26, 28 November 2013
Trisomy 13 is a genetic condition where the indiviual inhereits an extra copy of chromosome 13. It is also known as patau syndrome and affects around 1 in every 10,000 births. Over 80% of babies born with the condition will die before their first birthday.
The extra genetic material leads to many develeopmental problems. Symptoms can include: cleft lip and palate, seizures, congenital heart disease, decreased muscle tone, severe intellectual disability, low set ears and extra fingers or toes.