Diagnosis

This disease can be diagnosed during pregnancy if the doctor sees signs of this
disorder. The doctor will then proceed in testing the baby's DNA through the
mother's blood stream. If you suspect you or a family member has this disease your
local pediatrician will then be able to run lab test to analyze your /there
chromosomes to specialize the karyotypes to look for any missing x chromosomes.
There are also two other ways to diagnose one is chorionic villus sampling which
involves of a small piece of tissue from the placenta. The last one is amniocentesis
this test samples amniotic fluid from the uterus.