【摘 要】
：
脊髓空洞症 (Syringomy L ia)是一种缓慢进展性脊髓变性疾病 ,临床不少见 ,但父子同患且空洞巨大者临床罕见。先证者其父 ,4 3岁 ,右上肢、右胸脊麻木 2 0年 ,双上肢肌萎缩 1
【机 构】
：
聊城市第三人民医院,聊城市第三人民医院 山东聊城252000,山东聊城252000
论文部分内容阅读
脊髓空洞症 (Syringomy L ia)是一种缓慢进展性脊髓变性疾病 ,临床不少见 ,但父子同患且空洞巨大者临床罕见。先证者其父 ,4 3岁 ,右上肢、右胸脊麻木 2 0年 ,双上肢肌萎缩 10年、加重 2年。二便功能正常。查体 :眼底正常 ,颅神经正常 ,右颈 2—胸 6半马褂型痛 ,温觉丧失 ,触觉
Syringomyelia (Syringomy L ia) is a slow progressive spinal degenerative disease, clinical is not uncommon, but the father and son with the disease and the huge hole is clinically rare. The proband’s father, 43 years old, right upper limb, right thoracic numbness 20 years, double upper extremity muscle atrophy for 10 years, increased 2 years. Second, normal function. Physical examination: normal fundus, normal cranial nerves, right chest 2- chest 6 half-coat type pain, loss of temperature, touch
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