Congenital adrenal hyperplasia (CAH) and Williams Syndrome (WS; MIM # 194050) are distinct genetic conditions characterized by unique clinical features. 21-Hydroxylase deficiency (21-OHD; MIM #201910). the most common form of CAH. arises from mutations in the CYP21A2 gene. https://lockdownsecuritycanada.shop/product-category/obdii-t-harness/