Hip dysplasia associated with a hereditary sensorimotor polyneuropathy mimics a myopathic process

被引:1
作者
Hadianfard, Mohammad Javad [1 ]
Ashraf, Alireza [1 ,2 ]
机构
[1] Shiraz Univ Med Sci, Dept Phys Med & Rehabil, Shiraz, Iran
[2] Shiraz Univ Med Sci, Burn Res Ctr, Shiraz, Iran
关键词
Charcot-Marie-Tooth disease; hereditary motor and sensory neuropathy; hip dysplasia; MARIE-TOOTH-DISEASE;
D O I
10.4103/0972-2327.99722
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Some orthopedic complications have been reported in the hereditary neuropathies. However, the association of the hip dysplasia with this category of neuropathy is rarely recognized. We present a 13-year-old boy with the progressive weakness of the lower extremities, difficulty in walking, climbing stairs, and rising from floor; a wide-based, hyper-extended and waddling gait similar to a myopathic process. Hip radiography showed dysplastic acetabulae with hip subluxation, broken Shentons lines, and valgus femoral necks. In electrodiagnosis, there was a significant neuropathic process (absent all evoked sensory potentials, abnormal evoked motor responses, and neurogenic electeromyography) which eventually was found to be a hereditary mixed axonal and demyelinating sensorimotor polyneuropathy with concomitant hip dysplasia confirmed with thorough physical examination and the electrodiagnostic study. In patients with gait difficulties such as waddling gait mimicking a myopathic process, hereditary polyneuropathy complicated with hip dysplasia should be considered as well.
引用
收藏
页码:211 / 213
页数:3
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