Mimouni M, Kaufman H, Roitman A, Morag C, Sadan N
Eur J Pediatr. 1985 Jan;143(3):231-3. doi: 10.1007/BF00442149.
A female newborn infant with ambiguous genitalia was found to have hypertension (121/82 mm Hg) immediately after birth. The plasma testosterone (T) (0.73 nmol/l), delta 4-androstenedione (delta 4-A) (5.9 nmol/l), dehydroepiandrosterone (DHEA) (8.9 nmol/l), as well as 17 OH-hydroxyprogesterone (17 OHP) (152 nmol/l) were elevated. The diagnosis of 11 beta-hydroxylase deficiency was finally established on the basis of elevated plasma eleven-deoxycortisol (compound S) (greater than 0.6 mumol/l) and confirmed by the normalisation of the blood pressure during hydrocortisone therapy. Our case is probably the youngest patient with 11 beta-hydroxylase deficiency in whom the hypertension was found at birth.
一名患有生殖器模糊的女新生儿在出生后立即被发现患有高血压(121/82毫米汞柱)。血浆睾酮(T)(0.73纳摩尔/升)、δ4-雄烯二酮(δ4-A)(5.9纳摩尔/升)、脱氢表雄酮(DHEA)(8.9纳摩尔/升)以及17-羟孕酮(17 OHP)(152纳摩尔/升)均升高。最终根据血浆11-脱氧皮质醇(化合物S)升高(大于0.6微摩尔/升)确诊为11β-羟化酶缺乏症,并通过氢化可的松治疗期间血压恢复正常得到证实。我们的病例可能是出生时就发现高血压的最年轻的11β-羟化酶缺乏症患者。