A 33-year-old female 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
1 doctor answer • 3 doctors weighed in
Pediatrics 46 years experience
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.
1.4k viewsReviewed >2 years ago
Last updated Apr 17, 2016
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