swyer syndrome การใช้

At this point it is usually possible for a physician to make a diagnosis of Swyer syndrome.
Offspring which inherit this Y chromosome will have Swyer syndrome, characterized by an XY karyotype and a female phenotype.
Swyer syndrome is an example of a condition in which an externally unambiguous female body carries dysgenetic, atypical, or abnormal gonads.
A diagnosis of CAIS or Swyer syndrome can be made in utero by comparing a karyotype obtained by amniocentesis with the external genitalia of the fetus during a prenatal ultrasound.
As girls'ovaries normally produce no important body changes before puberty, a defect of the reproductive system typically remains unsuspected until puberty fails to occur in people with Swyer syndrome.