首页> 外文OA文献 >Spontaneous puberty in 46,XX subjects with congenital lipoid adrenal hyperplasia. Ovarian steroidogenesis is spared to some extent despite inactivating mutations in the steroidogenic acute regulatory protein (StAR) gene.
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Spontaneous puberty in 46,XX subjects with congenital lipoid adrenal hyperplasia. Ovarian steroidogenesis is spared to some extent despite inactivating mutations in the steroidogenic acute regulatory protein (StAR) gene.

机译:先天性脂质性肾上腺增生的46,XX名受试者的自发青春期。尽管类固醇生成的急性调节蛋白(StAR)基因发生了失活,但卵巢类固醇生成仍在一定程度上得以保留。

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摘要

Congenital lipoid adrenal hyperplasia (lipoid CAH) is the most severe form of CAH in which the synthesis of all gonadal and adrenal cortical steroids is markedly impaired. We report here the clinical, endocrinological, and molecular analyses of two unrelated Japanese kindreds of 46,XX subjects affected with lipoid CAH who manifested spontaneous puberty. Phenotypic female infants with 46,XX karyotypes were diagnosed with lipoid CAH as newborns based on a clinical history of failure to thrive, hyperpigmentation, hyponatremia, hyperkalemia, and low basal values of serum cortisol and urinary 17-hydroxycorticosteroid and 17-ketosteroid. These patients responded to treatment with glucocorticoid and 9alpha-fludrocortisone. Spontaneous thelarche occurred in association with increased serum estradiol levels at the age of 10 and 11 yr, respectively. Pubic hair developed at the age of 12 yr 11 mo in one subject and menarche was at the age of 12 yr in both cases. Both subjects reported periodic menstrual bleeding and subsequently developed polycystic ovaries. To investigate the molecular basis of the steroidogenic lesion in these patients, the StAR gene was characterized by PCR and direct DNA sequence analyses. DNA sequence analysis revealed that one patient is homozygous for the Gln 258 Stop mutation in exon 7 and that the other patient is a compound heterozygote with the Gln 258 Stop mutation and a single A deletion at codon 238 in the other allele causing a frame-shift, which renders the StAR protein nonfunctional. These findings demonstrate that ovarian steroidogenesis can be spared to some extent through puberty when the StAR gene product is inactive. This is in marked contrast to the early onset of severe defects in testicular and adrenocortical steroidogenesis which are characteristics of this disease.
机译:先天性类脂性肾上腺皮质增生(类脂性CAH)是最严重的CAH形式,其中所有性腺和肾上腺皮质类固醇的合成均明显受损。我们在这里报告两个自相亲的日本血亲,共46,XX名受脂性CAH感染而表现出自发青春期的日本亲属的临床,内分泌学和分子分析。根据未能to壮成长,色素沉着过多,血钠过低,血钾过高,血清皮质醇和尿液的基础值偏低以及尿液中的17-羟基皮质类固醇和17-酮类固醇的临床病史,将46,XX核型的表型女婴诊断为新生儿脂质体CAH。这些患者对糖皮质激素和9α-氟可的松的治疗有反应。自发性气肿分别与10岁和11岁时血清雌二醇水平升高有关。一名受试者在12岁11个月时出现阴毛,在两种情况下月经初潮都在12岁时。两名受试者均报告有月经周期出血,随后出现多囊卵巢。为了研究这些患者中类固醇生成病变的分子基础,通过PCR和直接DNA序列分析对StAR基因进行了表征。 DNA序列分析显示,一名患者是外显子7中Gln 258 Stop突变的纯合子,另一名患者是另一位等位基因中具有Gln 258 Stop突变和另一位密码子238缺失一个A的复合杂合子,致使StAR蛋白失去功能。这些发现表明,当StAR基因产物失活时,可以通过青春期在某种程度上保留卵巢类固醇生成。这与睾丸和肾上腺皮质类固醇生成的严重缺陷的早期发作形成鲜明对比,后者是该疾病的特征。

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