Department of Neurology, University of Oulu, Oulu, Finland.
Neuromuscul Disord. 2012 Oct 1;22 Suppl 2:S130-6. doi: 10.1016/j.nmd.2012.02.007.
Anoctaminopathy is a new muscular dystrophy caused by mutations in the ANO5 gene. ANO5 mutations cause distal and proximal phenotypes. We report here a follow-up muscle MRI study on five patients affected by distal form of anoctaminopathy. T1 weighted scans showed subsequent involvement of gastrocnemius medialis and soleus, hip adductors, hamstrings, gastrocnemius lateralis and quadriceps muscles, and later on tensor fascia lata, gluteus minimus and biceps brachii muscles, respectively. The STIR weighted images showed in the early stages widely distributed hyperintense signals, myoedema, in the adductors, hamstrings, and quadriceps muscles, which at that time have normal T1 signals. All patients showed asymmetry of muscle involvement both clinically and on muscle imaging. The progression of muscle involvement was relatively slow. We conclude that the pattern of muscle involvement seen in patients with distal myopathy with anoctamin 5 mutations (MMD3) is typical and can thus be useful during the differential diagnosis process allowing for a more targeted molecular approach.
钙激活氯离子通道病是一种由ANO5 基因突变引起的新型肌营养不良症。ANO5 突变导致远端和近端表型。我们在此报告 5 例远端型钙激活氯离子通道病患者的肌肉 MRI 随访研究结果。T1 加权扫描显示,跟腱内侧肌和比目鱼肌、髋关节内收肌、腘绳肌、腓肠肌外侧和股四头肌随后受累,随后分别累及阔筋膜张肌、小臀肌和肱二头肌。STIR 加权图像显示,在早期,内收肌、腘绳肌和股四头肌中广泛分布有高信号的肌水肿,此时 T1 信号正常。所有患者均表现出肌肉受累的临床和肌肉影像学不对称。肌肉受累的进展相对缓慢。我们的结论是,ANO5 基因突变导致的远端肌病(MMD3)患者的肌肉受累模式具有典型性,因此在鉴别诊断过程中具有一定的价值,有助于采取更有针对性的分子方法。