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.
Genes2Me offers the test which screens for mutations associated with 21 Hydroxylase defiency which is the most common cause of CAH.
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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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