MRI in DNM2-related centronuclear myopathy:: Evidence for highly selective muscle involvement

被引:49
作者
Schessl, Joachim
Medne, Livija
Hu, Ying
Zou, Yaqun
Brown, Mark J.
Huse, Jason T.
Torigian, Drew A.
Jungbluth, Heinz
Goebel, Hans-Hilmar
Boennemann, Carsten G. [1 ]
机构
[1] Univ Penn, Childrens Hosp Philadelphia, Sch Med, Div Neurol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Pathol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Radiol, Philadelphia, PA 19104 USA
[4] Univ London Imperial Coll Sci Technol & Med, Fac Med, Dubowitz Neuromuscular Ctr, Hammersmith Hosp, London, England
[5] St Thomas Hosp, Dept Paediat Neurol, Evelina Childrens Hosp, London, England
[6] Johannes Gutenberg Univ Mainz, Dept Neuropathol, D-6500 Mainz, Germany
关键词
centronuclear myopathy; dynamin; 2; MRI;
D O I
10.1016/j.nmd.2006.09.013
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Dynamin 2 has recently been recognized as a causative gene for the autosomal dominant form of centronuclear myopathy (dominant centronuclear myopathy). Here we report an affected father and daughter with dynamin 2 related AD CNM with predominantly distal onset of weakness. In addition to the diagnostic central location of myonuclei the muscle biopsy also showed core-like structures. Muscle MRI in the lower leg revealed prominent involvement of the soleus, but also of the gastrocnemius and the tibialis anterior whereas in the thigh there was a consistent pattern of selective involvement of adductor longus, semimembranosus, biceps femoris, rectus femoris, and vastus intermedius with relative sparing of vastus lateralis and medialis, sartorius, gracilis, and partly of the semitendinosus. These characteristic findings on muscle MRI confirm similar findings reported for CT imaging in dynamin 2 related dominant centronuclear myopathy and may help to differentiate this disorder from central core disease and other myopathies. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 32
页数:5
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