WHAT MUTATION CAUSES TRISOMY 13 SYNDROME

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Trisomy 13, also called Patau syndrome, is a chromosomal condition associated with severe intellectual disability and physical abnormalities in.

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Most cases of trisomy 13 are caused by random events during the full copies of chromosome 13 in each cell in the body, instead of the.

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Patau syndrome is the result of trisomy 13, meaning each cell in the body has three copies of chromosome 13 instead of the usual two.

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Causes. In individuals with Trisomy 13 Syndrome, all or a relatively large of developmentally important genes on chromosome

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Trisomy 13 is called "Patau syndrome," in honor of the physician who first described cell is forming, causing it to have an extra chromosome #18 or #13 inside.

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Trisomy What is it and what are the causes? Trisomy 13 is a genetic disorder that your baby gets when she has an extra 13th.

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Patau Syndrome - an article about the type of mutation that causes Patau syndrome - usually a chromosomal abnormality, trisomy

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Chromosomal abnormalities are responsible for miscarriages and stillbirths. Abnormalities can cause significant issues, including Down.

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Information for parents about trisomy 13, a rare genetic condition that causes developmental delay and affects many different organ systems.

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