CAH is a group of genetic conditions limiting hormone production from the adrenal glands. It affects a child's normal growth and development. Although it can be life-threatening, most people can lead normal lives with proper treatment.
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Genes2Me offers the test which screens for mutations associated with 21 Hydroxylase defiency which is the most common cause of CAH.
They are inherited in autosomal recessive manner i.e., two non-functional copies of the gene must be present for the disease to manifest. 21-hydroxylase deficiency (21-OHD) is the most common cause of congenital adrenal hyperplasia (CAH).
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