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WHAT IS CONGENITAL ADRENAL HYPERPLASIA (CAH)? Congenital Adrenal Hyperplasia (CAH) is a family of inherited disorders affecting the adrenal gland. Over 90% of those diagnosed with CAH are affected
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01
Obtain a DNA sample from the individual undergoing testing.
02
Select a laboratory to conduct the genetic testing.
03
Provide the necessary patient information and clinical history to the laboratory.
04
Await the results and interpretation of the genetic testing.
05
Consult with a genetic counselor or healthcare provider to discuss the implications of the genetic testing results.

Who needs genetics of congenital adrenal?

01
Individuals with suspected or diagnosed congenital adrenal hyperplasia (CAH) may need genetics testing to confirm the underlying genetic cause of the condition.
02
Family members of individuals with confirmed CAH may also benefit from genetics testing to determine their risk of inheriting the genetic mutation.
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Genetics of congenital adrenal refers to the study of genetic factors that contribute to the development of congenital adrenal conditions.
Medical professionals and researchers are typically required to file genetics of congenital adrenal.
Genetics of congenital adrenal can be filled out by providing relevant genetic information and test results.
The purpose of genetics of congenital adrenal is to better understand the genetic basis of congenital adrenal conditions and inform treatment and prevention strategies.
Information such as genetic test results, family history, symptoms, and treatment plans must be reported on genetics of congenital adrenal.
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