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杆状体肌病的肌肉磁共振成像

Magnetic resonance imaging of muscle in nemaline myopathy.

作者信息

Jungbluth Heinz, Sewry Caroline A, Counsell Serena, Allsop Joanna, Chattopadhyay Arijit, Mercuri Eugenio, North Kathryn, Laing Nigel, Bydder Graeme, Pelin Katarina, Wallgren-Pettersson Carina, Muntoni Francesco

机构信息

Department of Paediatric Neurology, Guy's Hospital, London, UK.

出版信息

Neuromuscul Disord. 2004 Dec;14(12):779-84. doi: 10.1016/j.nmd.2004.08.005.

Abstract

We report muscle MRI findings of 10 patients from 8 families with nemaline myopathy. Patients with involvement of the nebulin (NEB) gene showed a consistent pattern of selective muscle involvement corresponding to clinical severity. In mild cases, there was complete sparing of thigh muscles and selective involvement of tibialis anterior and soleus. In moderate cases, there was predominant involvement of rectus femoris, vastus lateralis and hamstring muscles and diffuse involvement of anterior compartment and soleus. Patients with nemaline myopathy secondary to mutations in the skeletal muscle alpha-actin (ACTA1) gene showed diffuse involvement of thigh and leg muscles with relative sparing of the gastrocnemii. Selective muscle involvement in both genetic categories was distinct from what has been reported in other congenital myopathies. We conclude that muscle MRI may be applied to distinguish nemaline myopathy from other conditions with similar clinical and histopathological features, to supplement clinical assessment in individual patients and to help direct genetic testing.

摘要

我们报告了来自8个家庭的10例杆状体肌病患者的肌肉MRI检查结果。涉及伴肌动蛋白(NEB)基因的患者表现出与临床严重程度相对应的选择性肌肉受累的一致模式。在轻症病例中,大腿肌肉完全未受累,仅胫骨前肌和比目鱼肌受累。在中度病例中,股直肌、股外侧肌和腘绳肌受累为主,前室和比目鱼肌弥漫性受累。继发于骨骼肌α-肌动蛋白(ACTA1)基因突变的杆状体肌病患者,大腿和小腿肌肉弥漫性受累,腓肠肌相对未受累。这两种遗传类型的选择性肌肉受累情况与其他先天性肌病的报道不同。我们得出结论,肌肉MRI可用于区分杆状体肌病与具有相似临床和组织病理学特征的其他疾病,以补充个体患者的临床评估并有助于指导基因检测。

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