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Q: The diagnosis of Down syndrome is made by examining the individual and?
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What are diagnosis for down syndrome?

Down syndrome IS the diagnosis.


What is the diagnosis if you have 92 chromosomes?

down's syndrome


What can be diagnosed by examining a karyotype of an individuals white blood cells?

A karyotype of an individual's white blood cells can be used to diagnose chromosomal abnormalities such as Down syndrome, Turner syndrome, and Klinefelter syndrome. It can also detect genetic disorders caused by aneuploidy or large structural chromosomal changes.


Is there a prenatal diagnosis or test for Down syndrome?

Yes there are examination that can determine that a fetus has down syndrome.. called amniocentesis.


What is the genetic complement of an individual with Down syndrome?

An individual with down syndrome has one extra chromosome beyond 2N. Down syndrome is designated trisomy 21 or 47,XX+21.


What is the diagnosis for Down syndrome?

It cannot be diagnosed, since it is in no way possible to contract.


Is it possible for an individual with Down syndrome to have offspring without it?

No, because people with Down syndrome can't have children.


What does an individual with an extra copy of chromosome 21 demonstrait traits of having?

down syndrome


What effects on an individual does downs syndrome cause?

Down syndrome mainly affects the persons physical features but it also affects their learning abilities.


Difference between the chromosomes of a person with Down syndrome and a person without Down syndrome?

An individual with Down Syndrome has the presence of all or part of an extra 21st chromosome.


Is a short Femur a sign of Down Syndrome?

A short femur can be a soft marker for Down Syndrome when detected during prenatal ultrasound screening, but it is not a definitive diagnosis. Down Syndrome is typically confirmed through genetic testing. Short femur measurements alone are not enough to diagnose Down Syndrome. It is important to consult with a healthcare provider for further evaluation and testing.


Is high risk of Down syndrome mean that the baby has it?

No. Both the scan and the blood test just give a higher or lower risk of Down's syndrome based on your age. For a diagnosis you will have to have an amniocentesis. You need to talk with your doctor, a counsellor and your partner to work out your next step.