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Selective pattern of muscle involvement seen in distal muscular dystrophy associated with anoctamin 5 mutations: A follow-up muscle MRI study

机译:在远端肌肉营养不良中与八环素5突变相关的选择性肌肉受累模式:后续肌肉MRI研究

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摘要

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.
机译:缺盐症是由ANO5基因突变引起的新型肌营养不良症。 ANO5突变会导致远端和近端表型。我们在此报告了对5例受远端形式的蛋氨酸病影响的患者的随访肌肉MRI研究。 T1加权扫描显示随后累及腓肠肌内侧和比目鱼肌,髋内收肌,绳肌,腓肠肌外侧肌和股四头肌,随后分别累及张弛筋膜,臀小肌和肱二头肌。 STIR加权图像显示,在早期,内收肌,绳肌和股四头肌中分布广泛的高强度信号,肌水肿,当时这些信号具有正常的T1信号。所有患者在临床上和在肌肉成像上均显示出肌肉受累的不对称性。肌肉受累的进展相对较慢。我们得出的结论是,在具有八分蛋白5突变(MMD3)的远端肌病患者中看到的肌肉受累模式是典型的,因此在鉴别诊断过程中很有用,从而可以采用更具针对性的分子方法。

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