Department of Neurology and Research Institute of Neuromuscular and Neurodegenerative Diseases, Qilu Hospital, Cheeloo College of Medicine, Shandong University, Jinan, 250012, Shandong, China.
Key Laboratory for Experimental Teratology of the Ministry of Education and Department of Medical Genetics, School of Basic Medical Sciences, Shandong University, Jinan, 250012, Shandong, China.
Neurogenetics. 2021 Mar;22(1):1-10. doi: 10.1007/s10048-020-00623-4. Epub 2020 Aug 6.
Distal myopathies are a group of clinically and genetically heterogeneous hereditary muscle disorders characterized by progressive muscular weakness starting in the distal parts of the limbs. The most common subtype of distal myopathy is GNE myopathy, a rare muscle disease with autosomal recessive inheritance. Limb-girdle muscular dystrophy 2G (LGMD2G) is a rare autosomal recessive subtype of LGMDs caused by TCAP variant. Patients with LGMD2G can present with distal myopathy and rimmed vacuoles on muscle pathology. Thus far, the most reported TCAP mutations related to LGMD2G were recessive frameshift or nonsense variants. Here, we described four Chinese patients from unrelated families with LGMD2G due to TCAP mutations. The clinical symptoms of our patients were similar to those previously reported in LGMD2G patients. Three different pathogenic TCAP variants were identified in these patients, including two frameshift variants and one intronic variant. Autophagolysosomes have been observed in one patient by electron microscopy. Our research expands the genetic spectrum of TCAP mutations in China, indicating c.165-166insG is likely the common pathogenic variant. We also provide evidences that autophagy may be involved in the pathophysiology of LGMD2G.
远端型肌病是一组临床和遗传异质性的遗传性肌肉疾病,其特征是四肢远端进行性肌无力。远端型肌病中最常见的亚型是 GNE 肌病,这是一种罕见的常染色体隐性遗传的肌肉疾病。肢带型肌营养不良 2G(LGMD2G)是一种罕见的常染色体隐性遗传的 LGMD 亚型,由 TCAP 变异引起。LGMD2G 患者可出现远端型肌病和肌病理上的边缘空泡。迄今为止,与 LGMD2G 相关的最常见的 TCAP 突变是隐性移码或无义变异。在此,我们描述了来自 4 个无血缘关系的中国家庭的 4 名 LGMD2G 患者,这些患者均存在 TCAP 突变。我们患者的临床症状与先前报道的 LGMD2G 患者相似。在这些患者中发现了 3 种不同的致病性 TCAP 变异,包括 2 种移码变异和 1 种内含子变异。通过电子显微镜观察到 1 名患者存在自噬溶酶体。我们的研究扩展了中国 TCAP 突变的遗传谱,提示 c.165-166insG 可能是常见的致病性变异。我们还提供了证据表明自噬可能参与了 LGMD2G 的病理生理学过程。