Phillipou G, Higgins B A
J Steroid Biochem. 1985 Mar;22(3):435-6. doi: 10.1016/0022-4731(85)90451-0.
A steroid disorder is described in two sisters, aged 13 and 17 years, in which the metabolism of cortisol results almost exclusively in urinary excretion of tetrahydro-cortisone (11-keto) derivatives. The evidence implies the existence of a deficiency in the peripheral enzymatic conversion of cortisone to cortisol.
在两名分别为13岁和17岁的姐妹中描述了一种类固醇疾病,其中皮质醇的代谢几乎完全导致四氢可的松(11-酮)衍生物经尿液排泄。证据表明存在可的松在外周酶促转化为皮质醇的缺陷。