Genetic Advisoring

("Genetic counseling and," 2009)


people who have CAH in their family history should be tested to see if a potential carrier. If a child is found affected with this disease, it can lead to potential genetic testing for other relatives of the family seeing if they are potential carriers.


If both parents are potential carriers and the wife is pregnant, they have two options to seeing if their child is affected by CAH. 

Chorionic villus sampling (CVS) is a procedure that obtains fetal cells by sampling cells from the developing placenta. This is done with ultrasound guidance to see the physical structures of the patient and fetus. 

Or

Amniocentesis, This procedure requires that a thin needle is passed through the abdomen, under ultrasound guidance, into the fluid filled sac that surrounds the fetus. Both are offered at 10-12 weeks after last menstrual period. 

- If a female fetus tests positive for CAH, then the mother can begin dexamethasone treatment. This treatment can help reduce masculinization of the female genitalia.