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NR0B1(DAX1)基因的新型移码突变导致两名高个成年兄弟患病。

Novel frameshift mutation of the NR0B1(DAX1) in two tall adult brothers.

机构信息

1st Department of Pediatrics, Semmelweis University, Bókay J Street 53-54, Budapest, 1083, Hungary.

Csolnoky Ferenc Hospital, Kórház Street 1, Veszprém, 8200, Hungary.

出版信息

Mol Biol Rep. 2019 Aug;46(4):4599-4604. doi: 10.1007/s11033-019-04688-9. Epub 2019 Jul 6.

Abstract

NR0B1 (nuclear receptor subfamily 0, group B, member 1) is a transcription factor encoded by DAX1 (dosage-sensitive sex reversal, adrenal hypoplasia critical region, on chromosome X, gene 1) responsible for the development and maintenance of the steroidogenic tissues. In humans the DAX1 mutations cause congenital adrenal hypoplasia (AHC) and hypogonadotropic hypogonadism (HHG) in boys. Here we report two brothers who were assessed by endocrinologist at the age of 51 and 43 because of their serious osteoporosis. They had been substituted with prednisolone since the age of 4 and 9 years because of their primary adrenal insufficiency (PAI). Due to their late puberty caused by HHG at the age of 16 and 17 years their heights were - 3.1 and - 3.3 SD, but then they had a significant growth during their adulthood and reached the + 1.85 SD and + 3.78 SD respectively. During this period, they received glucocorticoid supplementation, but the treatment of their HHG was inadequate. At the age of 51 and 43 years insulin tolerance test (ITT) and gonadotropin releasing hormone (GnRH) test confirmed their PAI and HHG. Genetic test performed at this time revealed a novel, four nucleotides deletion (del.586-571c.GGGC or 572-575c.GGGC) of DAX1 gene. The two brothers with AHC and HHG caused by a novel DAX1 mutation, reached tall final heights, despite of the disadvantageous prednisolone treatment during their childhood. We assume that the long-term lack of the sexual hormone substitution was a significant reason of their above average height as well as their serious osteoporosis.

摘要

NR0B1(核受体亚家族 0,B 组,成员 1)是由 DAX1(剂量敏感性别逆转,肾上腺发育不全关键区,X 染色体,基因 1)编码的转录因子,负责类固醇生成组织的发育和维持。在人类中,DAX1 突变导致先天性肾上腺发育不全(AHC)和促性腺激素缺乏性性腺功能减退症(HHG)在男孩中。在这里,我们报告了两个兄弟,他们因严重骨质疏松症在 51 岁和 43 岁时由内分泌医生评估。由于他们的原发性肾上腺功能不全(PAI),他们从 4 岁和 9 岁开始就一直在使用泼尼松龙替代治疗。由于他们在 16 岁和 17 岁时因 HHG 导致青春期延迟,他们的身高分别为-3.1 和-3.3 SD,但随后在成年期有显著增长,分别达到+1.85 SD 和+3.78 SD。在此期间,他们接受了糖皮质激素补充治疗,但 HHG 的治疗不足。在 51 岁和 43 岁时,胰岛素耐量试验(ITT)和促性腺激素释放激素(GnRH)试验证实了他们的 PAI 和 HHG。此时进行的基因测试显示 DAX1 基因发生了一个新的四核苷酸缺失(del.586-571c.GGGC 或 572-575c.GGGC)。这两个患有 AHC 和 HHG 的兄弟,尽管在儿童期接受了不利的泼尼松龙治疗,但最终身高仍很高。我们假设长期缺乏性激素替代是导致他们身高高于平均水平以及严重骨质疏松症的一个重要原因。

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