Ajlouni K M, Arnaout M A, Qoussous Y
Department of Internal Medicine, Faculty of Medicine, Jordan University of Science and Technology, Irbid.
J Endocrinol Invest. 1996 May;19(5):316-9. doi: 10.1007/BF03347869.
Classic congenital 11-beta-hydroxylase deficiency is a relatively uncommon cause of congenital adrenal hyperplasia and is characterized by virilization and often hypertension. The association of skeletal abnormalities (short metatarsal bone) and pulmonary stenosis in a patient with 11-beta-hydroxylase has been reported by our group. In this report, three new patients with congenital adrenal hyperplasia due to a defect in 11-beta-hydroxylase enzyme with short fourth metatarsals are described. Gynecomastia was noted in one patient. The relative rarity of 11-beta-hydroxylase deficiency and the association of skeletal abnormalities suggest the possibility that this is more than a mere coincidental finding.
经典型先天性11-β-羟化酶缺乏症是先天性肾上腺皮质增生症相对少见的病因,其特征为男性化,且常伴有高血压。我们团队曾报道过1例患有11-β-羟化酶缺乏症的患者合并骨骼异常(第四跖骨短小)及肺动脉狭窄。在本报告中,描述了3例因11-β-羟化酶缺陷导致先天性肾上腺皮质增生症且第四跖骨短小的新患者。其中1例患者出现了男性乳房发育。11-β-羟化酶缺乏症相对罕见,以及骨骼异常与之相关,提示这可能不仅仅是一个偶然发现。