部分 3β- 羟类固醇脱氢酶 2 型缺乏症的晚期诊断--一种新基因变异的特征。

IF 0.7 Q4 ENDOCRINOLOGY & METABOLISM
Cagla Margit Øzdemir, Mette Mølby Nielsen, Jani Liimatta, Clarissa D Voegel, Rawda Naamneh Elzenaty, Victor S Wasehuus, Marie Lind-Holst, Marie Juul Ornstrup, Stine Bjørn Gram, Lilian Bomme Ousager, Christa E Flück, Claus H Gravholt
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引用次数: 0

摘要

摘要:先天性肾上腺增生症(CAH)是最常见的遗传性罕见内分泌疾病之一。本病例报告了两个女性兄弟姐妹,尽管她们很早就入院,并有明显的CAH表现,如感染、多毛、月经紊乱和多囊卵巢综合征(PCOS)表型,但却被延迟诊断为非典型CAH 3β-羟类固醇脱氢酶2型(3βHSD2D/HSD3B2)。最初,妹妹 1 被误诊为多囊卵巢综合症,后来又根据超声波检查和生化检查结果被误诊为 11-羟化酶缺乏症(CYP11B1),21-羟化酶缺乏症(CYP21A2)基因检测结果为阴性。当妹妹 2 号也出现雄激素过多症状时,又进行了诊断性检查。CAH/ 类固醇紊乱的基因检测最终发现,两兄妹都是 HSD3B2 基因两个变体的复合杂合子:一个是帧移变体 c.558dup,p.(Thr187Hisfs*17),另一个是新型错义变体 c.65T>C,p.(Leu22Ser)。Synacthen 试验显示皮质醇增加不足。在细胞模型中对这些变异体进行的体外研究显示,p.(Thr187Hisfs*17)变异体丧失功能,p.(Leu22Ser)变异体具有部分活性,这证实了该变异体为非经典 CAH。症状重叠和缺乏有关类固醇生物合成及相关罕见 CAH 形式的专业知识可能是诊断延迟的原因。然而,随着诊断方法的更新,偏倚性降低,非常罕见的非经典 CAH 将不再被忽视:学习要点:非经典 3βHSD2 可能诊断不足。轻度非经典 3βHSD2 的晚期诊断确实存在,人们应该对这种诊断有所了解。早期诊断 NCCAH 可避免许多后果,如严重多毛症、长期月经不调、不孕不育,甚至是伴有严重感染的肾上腺危象。应尽早进行综合类固醇分析和基因检测,尤其是在对诊断有疑问时。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Late diagnosis of partial 3β-hydroxysteroid dehydrogenase type 2 deficiency - characterization of a new genetic variant.

Summary: Congenital adrenal hyperplasia (CAH) is one of the most common inherited rare endocrine disorders. This case report presents two female siblings with delayed diagnosis of non-classical CAH 3β-hydroxysteroid dehydrogenase type 2 (3βHSD2D/HSD3B2) despite early hospital admission and apparent CAH manifestations such as infections, hirsutism, menstrual disturbances, and PCOS phenotype. Initially, sister 1 was misdiagnosed with PCOS and then 11-hydroxylase deficiency (CYP11B1), based on ultrasound, biochemical findings, and negative genetic testing for 21-hydroxylase deficiency (CYP21A2). Additional diagnostic workup was performed when sister 2also presented with symptoms of androgen excess. Genetic testing for CAH/steroid disorders finally revealed that both siblings were compound heterozygous for two variants in the HSD3B2 gene: a frameshift variant, c.558dup, p.(Thr187Hisfs*17) and a novel missense variant, c.65T>C, p.(Leu22Ser). A Synacthen test showed an insufficient cortisol increase. In vitro studies of the variants in a cell model revealed loss of function for the p.(Thr187Hisfs*17) and partial activity for p.(Leu22Ser) confirming non-classic CAH. Overlapping symptomatology and lack of specialized knowledge on steroid biosynthesis and associated rarest forms of CAH may explain the delayed diagnosis. However, with newer diagnostic methods comprising a less biased approach, very rare forms of non-classical CAH may no longer be overlooked in the future.

Learning points: Non-classic 3βHSD2 is likely underdiagnosed. Late diagnosis of mild non-classic 3βHSD2 does occur and one should be aware of this diagnosis. Early diagnosis of NCCAH may prevent many consequences such as severe hirsutism, prolonged menstrual irregularities, infertility, or even adrenal crisis with severe infections. Comprehensive steroid profiling and genetic testing should be used earlier, especially when in doubt about a diagnosis.

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来源期刊
CiteScore
1.50
自引率
0.00%
发文量
142
审稿时长
9 weeks
期刊介绍: Endocrinology, Diabetes & Metabolism Case Reports publishes case reports on common and rare conditions in all areas of clinical endocrinology, diabetes and metabolism. Articles should include clear learning points which readers can use to inform medical education or clinical practice. The types of cases of interest to Endocrinology, Diabetes & Metabolism Case Reports include: -Insight into disease pathogenesis or mechanism of therapy - Novel diagnostic procedure - Novel treatment - Unique/unexpected symptoms or presentations of a disease - New disease or syndrome: presentations/diagnosis/management - Unusual effects of medical treatment - Error in diagnosis/pitfalls and caveats
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