Suppr超能文献

晚发性钴胺素 C 缺陷 (cb1C) 的独特临床、神经影像学和遗传学特征:16 例中国病例报告。

Distinct clinical, neuroimaging and genetic profiles of late-onset cobalamin C defects (cb1C): a report of 16 Chinese cases.

机构信息

Department of Neurology, Xuanwu Hospital, Capital Medical University, 45 Changchun Street, Xicheng District, Beijing, 100053, People's Republic of China.

Department of Radiology, Xuanwu Hospital, Capital Medical University, Beijing, China.

出版信息

Orphanet J Rare Dis. 2019 May 15;14(1):109. doi: 10.1186/s13023-019-1058-9.

Abstract

OBJECTIVE

The importance of late-onset cobalamin C (cblC) disorder is underestimated in adults. Improved awareness on its clinical and neuroimaging features helps timely diagnosis and appropriate treatment.

METHODS

Totally 16 late-onset cblC cases were diagnosed based on clinical, biochemical findings and MMAHC gene mutation analysis. Clinical presentations, neuroimaging features and mutational spectrum were reviewed.

RESULTS

The case series included 10 males and 6 females, with average age of 22 (range 13-40) years. All the 16 patients displayed bilateral pyramidal tract signs, and most of the cases (13) had cognitive impairment. Other symptoms included psychiatric symptoms (6), epilepsy (6), peripheral nerve damage (5), ocular symptoms (4) and lower-limb thrombosis (1). The neuroimaging findings were dominated by cerebral atrophy (11/16), followed by white matter lesions (4), cerebellar lesions/atrophy (2) and spinal cord lesions (1). There were also 2 patients with normal imaging. All the MMACHC mutations were compound heterozygous, of which the most and second frequent was c.482G > A (p.R161Q; 15/16 case; allele frequency: 46.88%) and c.609G > A(p.W203X; 6/16 case; allele frequency: 18.75%). In addition, patients carrying frameshift mutations (deletion/duplication) presented more frequently with psychiatric symptoms (57.1%) and optic nerve damages (42.9%) than those carrying point mutations (22.2 and 11.1%, respectively). In contrast, peripheral nerve (44.4%) and white matter lesions (33.3%) were more frequently identified in point mutation- carriers. However, the differences did not achieve statistical significance (all p > 0.05).

CONCLUSION

Compared to the early-onset form, late-onset cblC displayed some clinical, neuroimaging and mutational profiles, which warrants particular attention in adult neurologic practice. These findings not only broaden our insights into the genotypes and phenotypes of the disease, but highlight the importance of early diagnosis and initiation of appropriate treatments.

摘要

目的

成人中钴胺素 C(cblC)迟发型疾病的重要性被低估。提高对其临床和神经影像学特征的认识有助于及时诊断和适当治疗。

方法

根据临床、生化发现和 MMAHC 基因突变分析,共诊断出 16 例迟发性 cblC 病例。回顾了临床特征、神经影像学特征和突变谱。

结果

该病例系列包括 10 名男性和 6 名女性,平均年龄为 22 岁(范围 13-40 岁)。所有 16 例患者均表现为双侧锥体束征,大多数患者(13 例)存在认知障碍。其他症状包括精神症状(6 例)、癫痫(6 例)、周围神经损伤(5 例)、眼部症状(4 例)和下肢血栓形成(1 例)。神经影像学表现以脑萎缩为主(11/16),其次为白质病变(4)、小脑病变/萎缩(2)和脊髓病变(1)。还有 2 例患者影像学正常。所有 MMACHC 突变均为复合杂合突变,其中最常见和第二常见的是 c.482G>A(p.R161Q;16 例中的 15 例;等位基因频率:46.88%)和 c.609G>A(p.W203X;16 例中的 6 例;等位基因频率:18.75%)。此外,携带移码突变(缺失/重复)的患者比携带点突变的患者更常出现精神症状(57.1%)和视神经损伤(42.9%)(分别为 22.2%和 11.1%)。相反,点突变携带者更常出现周围神经病变(44.4%)和白质病变(33.3%)。然而,差异没有统计学意义(均 p>0.05)。

结论

与早发型相比,迟发型 cblC 具有一些临床、神经影像学和突变特征,这在成人神经病学实践中需要特别注意。这些发现不仅拓宽了我们对疾病基因型和表型的认识,而且强调了早期诊断和及时开始适当治疗的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b505/6521494/80334821adef/13023_2019_1058_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验