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CMT4J 患者的临床和遗传特征。

Clinical and genetic features of patients suffering from CMT4J.

机构信息

Reference Center for Neuromuscular Disorders and ALS, Timone University Hospital, Aix-Marseille University, 264 Rue Saint Pierre, 05 13385, Marseille, Cedex, France.

Filnemus, European Reference Network of Rare Diseases (ERN), Marseille, France.

出版信息

J Neurol. 2024 Mar;271(3):1355-1365. doi: 10.1007/s00415-023-12076-4. Epub 2023 Nov 11.

Abstract

Mutations in the FIG4 gene have been identified in various diseases, including amyotrophic lateral sclerosis, Parkinson's disease, and Charcot-Marie-Tooth 4 J (CMT4J), with a wide range of phenotypic manifestations. We present eight cases of CMT4J patients carrying the p.Ile41Thr mutation of FIG4. The patients were categorized according to their phenotype. Six patients had a pure CMT; whereas, two patients had a CMT associated with parkinsonism. Three patients had an early onset and exhibited more severe forms of the disease. Three others experienced symptoms in their teenage years and had milder forms. Two patients had a late onset in adulthood. Four patients showed electrophysiological evidence of conduction blocks, typically associated with acquired neuropathies. Consequently, two of them received intravenous immunoglobulin treatment without a significant objective response. Interestingly, two heterozygous patients with the same mutations exhibited contrasting phenotypes, one having a severe early-onset form and the other experiencing a slow disease progression starting at the age of 49. Notably, although 7 out of 8 patients in this study were compound heterozygous for the p.Ile41Thr mutation, only one individual was found to be homozygous for this genetic variant and exhibited an early-onset, severe form of the disease. Additionally, one patient who developed the disease in his youth was also diagnosed with hereditary neuropathy with pressure palsies. Our findings provide insights into the CMT4J subtype by reporting on eight heterogeneous patient cases and highlight the potential for misdiagnosis when conduction blocks or asymmetrical nerve conduction study results are observed in patients with FIG4 mutations.

摘要

FIG4 基因突变已在多种疾病中被发现,包括肌萎缩侧索硬化症、帕金森病和 Charcot-Marie-Tooth 4J(CMT4J),具有广泛的表型表现。我们报告了 8 例携带 FIG4 蛋白 p.Ile41Thr 突变的 CMT4J 患者。这些患者根据其表型进行了分类。6 例为单纯 CMT;而 2 例为伴有帕金森病的 CMT。3 例患者发病年龄较早,疾病表现更为严重。另外 3 例在青少年时期出现症状,表现较轻。2 例患者成年后发病较晚。4 例患者有神经传导阻滞的电生理证据,通常与获得性神经病相关。因此,其中 2 例接受了静脉注射免疫球蛋白治疗,但没有明显的客观反应。有趣的是,2 例携带相同突变的杂合子患者表现出截然不同的表型,1 例为严重的早发型,另 1 例为 49 岁时开始缓慢进展的疾病。值得注意的是,尽管本研究中的 8 例患者中有 7 例为 p.Ile41Thr 突变的复合杂合子,但只有 1 例患者为纯合子,表现为早发型、严重的疾病形式。此外,1 例年轻时发病的患者还被诊断为遗传性压力易发性神经病。我们的发现通过报告 8 例异质性患者病例,为 CMT4J 亚型提供了深入了解,并强调了当 FIG4 基因突变患者出现传导阻滞或不对称性神经传导研究结果时,可能会导致误诊。

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