“…The measurement of serum 17-0HP concentrations as an alternative to urinary pregnanetriol excretion (Bongiovanni and Clayton, 1954;Morris, 1959) or the ll-oxygenation index (Hill, 1960;Edwards et al, 1964) has been reported for the diagnosis of patients with congenital adrenal hyperplasia due to Zl-hydroxylase deficiency (Strott et al, 1969;Pham-Huu-Trung et al, 1973), and, with some rare exceptions , pregnanetriol in urine reflects this excessive production of 17-0HP. The detection of a diminished 21-hydroxylase activity in the non-salt losing form of the disease in children and adults can be revealed by ACTH stimulation and concurrent measurement of blood levels of 17-0HP or pregnanetriol in urine Barnes and Atherden, 1972;Givens et al, 1975;Newmark et al, 1977;Parth et al, 1978).…”