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A member asked:
3 early mcs & chromosomal abnrml in all fetuses (no birth), is karyotyping of parents the only genetic testing tht can be done? names of any other pls
A doctor has provided 1 answer
It's the starting pt: Parent study comes first.A person can appear normal if they carry all the proper chromosome material but with part belonging to one chromosome swapped with another.(ie, part of a #15 is on #21) When fertilization occurs, the fetus may get part of the mistake and not the other & be defective.Some of these have a partial chance of normal birth, some would always end up a defect.See a geneticist.
Answered 4/17/2016
1.4k views
Related Questions
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I had sub chorionic hemorrhage, single umblical artery n spinq bifida during preg. R these 3 due to chromosomal disorder. Is karyotyping is necessary?
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Are there karyotyping like genetic level tests to confirm if a couple is compatible & will certainly have healthy children if they plan for pregnency?
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Wife pregnancy was terminated in 3rd month and karyotyping shows chromosomal analysis of poc is found abnormal 47, --+21. Is it will solve next time ?
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How common is it for insurance to pay for genetic testing if I want to get it done for a hereditary birth disease?
2 doctors weighed in across 2 answers
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