cah congenital adrenal hyperlasia 11 mutations
Sample Type: Peripheral blood EDTA vacutainer(3ml)
Reporting Time: 7-10 days
This test can uncover cah congenital adrenal hyperlasia 11 mutations.These symptoms may be due to such things as race, dietetic preference, age, sex, menstrual cycle, degree of physical activity, problems with collection and/or handling of the specimen, non-prescription drugs (aspirin, cold medications, vitamins, etc.), prescription drugs, alcohol intake and a number of non-illness-related factors. Any cah congenital adrenal hyperlasia 11 mutations results should be discussed with your doctor or physician. It is not possible to diagnose or treat any disease or problem with this blood test alone.
This cah congenital adrenal hyperlasia 11 mutations test helpful in evaluating the status of an individual and help you to learn more about your body and detect potential problems in early stages when treatment or changes in personal habits can be most effective.cah congenital adrenal hyperlasia 11 mutations results can provide important clinical information to physicians or doctors to help patients make the right healthcare decisions for their particular risks