Introduction21-hydroxylase deficiency (21OHD) is the most common cause of congenital adrenal hyperplasia (CAH). However. patients with 21OHD manifest various phenotypes due to a wide-spectrum residual enzyme activity of different CYP21A2 mutations. MethodsA total of 15 individuals from three unrelated families were included in this study. https://www.jmannino.com/quick-offer-Viqua-F4-50-Plus-Monitored-UV-System-Powered-by-UVMax-15-gpm-230-Volt-on-sale/