Department of Endocrinology, First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, China.
Chin Med J (Engl). 2010 May 20;123(10):1264-8.
Steroid 11beta-hydroxylase deficiency (11beta-OHD), an autosomal recessive inherited disease, accounts for 5% - 8% of congenital adrenal hyperplasia. It was scarcely reported in China. This article reports two Chinese girls with 11beta-OHD.
The two patients were sisters and presented with hypertrichosis, skin pigmentation, laryngeal prominence and virilization of external genitalia. The patients were followed up for their clinical symptoms and signs, hormone profile, and adrenal image. The genomic deoxyribonucleic acids of the patients and their parents were isolated. 11beta-hydroxylase gene (CYP11B1) was amplified by polymerase chain reaction and directly sequenced.
Hormone tests showed that serum cortisol was in the low limit of normal range, whereas the concentrations of adrenocorticotropic hormone, testosterone and progesterone were much higher than those of normal adult females. There were obvious adrenal hyperplasia and advance of bone age. After 11 months of treatment with dexamethasone, the skin pigment became regressed; the breast, uterus and ovary gradually developed and normal menstrual cycle started while the manifestations of virilization did not change. A single point mutation of CYP11B1 (R454C, GGC --> TGC) in all the members of this family was detected. The sisters were homozygous and their parents were heterozygous.
The clinical manifestation of 11beta-OHD is complicated. The manifestation of virilization could not regress after treatment with dexamethasone. The novel missense mutation of CYP11B1 (R454C, GGC --> TGC) is the pathogenesis of 11beta-OHD at least in some Chinese patients.
类固醇 11β-羟化酶缺乏症(11β-OHD)是一种常染色体隐性遗传疾病,占先天性肾上腺皮质增生症的 5%-8%。在中国很少有报道。本文报告了两例中国女孩患 11β-OHD。
两名患者为姐妹,表现为多毛症、皮肤色素沉着、喉结突出和外生殖器男性化。对患者进行了临床症状和体征、激素谱和肾上腺影像学的随访。分离患者及其父母的基因组脱氧核糖核酸。采用聚合酶链反应直接扩增 11β-羟化酶基因(CYP11B1)并进行测序。
激素检测显示血清皮质醇处于正常范围下限,而促肾上腺皮质激素、睾酮和孕酮浓度明显高于正常成年女性。肾上腺明显增生,骨龄提前。用地塞米松治疗 11 个月后,皮肤色素沉着消退;乳房、子宫和卵巢逐渐发育,开始正常月经周期,而男性化表现无变化。在这个家族的所有成员中都检测到 CYP11B1 的单点突变(R454C,GGC-->TGC)。姐妹俩均为纯合子,父母均为杂合子。
11β-OHD 的临床表现复杂。用地塞米松治疗后,男性化表现不能消退。CYP11B1 的新错义突变(R454C,GGC-->TGC)是至少部分中国患者 11β-OHD 的发病机制。