A Novel Hemizygous ANOS1 Variant in a Patient With Kallmann Syndrome and Type 2 Diabetes Mellitus: A Case Report.

IF 0.8 Q4 ENDOCRINOLOGY & METABOLISM
Case Reports in Endocrinology Pub Date : 2026-07-22 eCollection Date: 2026-01-01 DOI:10.1155/crie/8624241
Si Qin, Yindi Zhang, Yanrong Chen, Wei Chen, Yinxing Ni, Jian Zhong
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引用次数: 0

Abstract

Introduction: Kallmann syndrome (KS), a rare genetic disorder, is characterized by congenital hypogonadotropic hypogonadism (CHH) and anosmia or hyposmia.

Case report: We report a case of KS with type 2 diabetes mellitus (T2DM) associated with a novel hemizygous missense variant in ANOS1 (NM_000216.4; exon 4; c.505G >C;p.(Gly169Arg)). A 33-year-old male presented with persistent hyperglycemia, delayed pubertal development with absent secondary sexual characteristics, and lifelong anosmia. Olfactory testing, magnetic resonance imaging (MRI) of the pituitary region, and a gonadotropin-releasing hormone (GnRH) stimulation test supported a clinical diagnosis of KS. Trio-based exome sequencing (ES) revealed the aforementioned hemizygous variant in ANOS1. Notably, neither parent harbored this variant, supporting a de novo origin, which is consistent with the variant's potential pathogenicity. Multiple sequence alignment showed that Gly169 is highly conserved across species, suggesting it may be functionally important for the protein. Furthermore, a three-dimensional protein model generated using SWISS-MODEL predicted marked conformational changes in the protein attributable to this amino acid substitution at a highly conserved residue, suggesting a potential functional impact. Notably, emerging evidence has linked ANOS1 variants to dysregulated glucose metabolism, supporting a potential association with T2DM in this case. For treatment, insulin and oral hypoglycemic agents were used for glycemic control, and a GnRH pump was initiated. At the sixth follow-up visit, the patient had achieved satisfactory glycemic control; however, serum testosterone levels remained low despite GnRH pump therapy, so testosterone replacement therapy was subsequently initiated.

Conclusions: ANOS1 variants are genetically diverse and may contribute to both KS pathogenesis and the development of comorbid T2DM, though further studies are needed to confirm this link. For KS patients, close monitoring of fasting glucose, glycated hemoglobin, and oral glucose tolerance test results is advisable to detect diabetes and prediabetes early.

在Kallmann综合征和2型糖尿病患者中发现一种新的半合子ANOS1变异:一例报告。
简介:卡尔曼综合征(Kallmann syndrome, KS)是一种罕见的遗传性疾病,以先天性促性腺功能低下(CHH)和嗅觉缺失或低嗅觉为特征。病例报告:我们报告了一例KS合并2型糖尿病(T2DM)与ANOS1 (NM_000216.4;外显子4;C . 505g >C;p.(Gly169Arg))的新型半合子错义变异相关的病例。33岁男性,表现为持续性高血糖,青春期发育迟缓,无第二性征,终生嗅觉缺失。嗅觉测试、垂体区磁共振成像(MRI)和促性腺激素释放激素(GnRH)刺激试验支持KS的临床诊断。三基外显子组测序(ES)在ANOS1中发现了上述半合子变异。值得注意的是,双亲都没有携带这种变体,支持从头起源,这与变体的潜在致病性一致。多重序列比对表明,Gly169在物种间高度保守,表明它可能对该蛋白具有重要的功能。此外,使用SWISS-MODEL生成的三维蛋白质模型预测,由于高度保守的残基上的氨基酸取代,蛋白质的构象发生了显著变化,表明可能对功能产生影响。值得注意的是,新出现的证据表明ANOS1变异与糖代谢失调有关,支持在这种情况下与2型糖尿病的潜在关联。治疗方面,使用胰岛素和口服降糖药控制血糖,并启动GnRH泵。第六次随访时,患者血糖控制满意;然而,尽管GnRH泵治疗,血清睾酮水平仍然很低,因此睾酮替代治疗随后开始。结论:ANOS1变异具有遗传多样性,可能与KS发病机制和共病T2DM的发展有关,但需要进一步的研究来证实这一联系。对于KS患者,建议密切监测空腹血糖、糖化血红蛋白和口服糖耐量试验结果,以便早期发现糖尿病和糖尿病前期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Case Reports in Endocrinology
Case Reports in Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.10
自引率
0.00%
发文量
45
审稿时长
13 weeks
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