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共济失调毛细血管扩张症样疾病患者出现高促性腺激素性性腺功能减退和多分叶中性粒细胞:潜在的诊断线索?

Hypergonadotropic hypogonadism and hypersegmented neutrophils in a patient with ataxia-telangiectasia-like disorder: potential diagnostic clues?

作者信息

Yoshida Takeshi, Awaya Tomonari, Shibata Minoru, Kato Takeo, Numabe Hironao, Kobayashi Junya, Komatsu Kenshi, Heike Toshio

机构信息

Department of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto, Japan.

出版信息

Am J Med Genet A. 2014 Jul;164A(7):1830-4. doi: 10.1002/ajmg.a.36546. Epub 2014 Apr 14.

DOI:10.1002/ajmg.a.36546
PMID:24733832
Abstract

Ataxia-telangiectasia-like disorder (ATLD) is a rare autosomal recessive disorder, and has symptoms similar to ataxia-telangiectasia (AT). ATLD is caused by mutations in the MRE11 gene, involved in DNA double-strand break repair (DSBR). In contrast to AT, ATLD patients lack key clinical features, such as telangiectasia or immunodeficiency, and are therefore difficult to be diagnosed. We report a female ATLD patient presenting with hypergonadotropic hypogonadism and hypersegmented neutrophils, previously undescribed features in this disorder, and potential diagnostic clues to differentiate ATLD from other conditions. The patient showed slowly progressive cerebellar ataxia from 2 years of age, and MRI revealed atrophy of the cerebellum, oculomotor apraxia, mild cognitive impairment, writing dystonia, hypergonadotropic hypogonadism with primary amenorrhea, and hypersegmented neutrophils. Western blot assay demonstrated total loss of MRE11 and reduction of ATM-dependent phosphorylation; thus, we diagnosed ATLD. Genetically, a novel missense mutation (c.140C>T) was detected in the MRE11 gene, but no other mutation was found in the patient. Our presenting patient suggests that impaired DSBR may be associated with hypergonadotropic hypogonadism and neutrophil hypersegmentation. In conclusion, when assessing patients with ataxia of unknown cause, ATLD should be considered, and the gonadal state and peripheral blood smear samples evaluated.

摘要

共济失调毛细血管扩张样疾病(ATLD)是一种罕见的常染色体隐性疾病,具有与共济失调毛细血管扩张症(AT)相似的症状。ATLD由参与DNA双链断裂修复(DSBR)的MRE11基因突变引起。与AT不同,ATLD患者缺乏关键临床特征,如毛细血管扩张或免疫缺陷,因此难以诊断。我们报告了一名女性ATLD患者,其表现为高促性腺激素性性腺功能减退和核分叶过多的中性粒细胞,这是该疾病以前未描述过的特征,也是将ATLD与其他疾病区分开来的潜在诊断线索。该患者从2岁起出现缓慢进展的小脑共济失调,MRI显示小脑萎缩、眼球运动失用、轻度认知障碍、书写性肌张力障碍、伴有原发性闭经的高促性腺激素性性腺功能减退以及核分叶过多的中性粒细胞。蛋白质印迹分析显示MRE11完全缺失以及ATM依赖性磷酸化减少;因此,我们诊断为ATLD。在基因方面,在MRE11基因中检测到一个新的错义突变(c.140C>T),但在该患者中未发现其他突变。我们的病例提示DSBR受损可能与高促性腺激素性性腺功能减退和中性粒细胞核分叶过多有关。总之,在评估病因不明的共济失调患者时,应考虑ATLD,并评估性腺状态和外周血涂片样本。

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