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进行性肌营养不良国内报告不少,但眼肌型少见。国内仅有沈氏(中华神经精神科杂志4(13):241 1980)报告8例,现报告一例如下。 陈某,男,25岁,1984年3月21日入院,患者10岁左右双眼睑下垂。于1978年(10年后)双睑下垂明显,视物不清,眼球活动受限,曾拟诊动眼神经麻痹症,行眼睑下垂矫正术。术后双眼睑下垂好转。此后每当“感冒”即有双眼红肿疼痛,经抗生素治疗好转。1979年因角膜云翳导致右眼失明,眼睑下垂加重,伴四肢无力,双上肢为著,且进行性加重,以至不能从事重体力劳动。既往史、家族史
Progressive muscular dystrophy a lot of domestic reports, but rare ocular muscle type. Only domestic Shen (Chinese Journal of Neurology and Psychiatry 4 (13): 241 1980) reported 8 cases, the report is an example below. Chen, male, 25 years old, admitted to hospital on March 21, 1984, the patient had a double eyelid ptosis about 10 years old. In 1978 (10 years later) double eyelid ptosis was obvious, blurred vision, eye activity is limited, had proposed oculomotor palsy, eyelid ptosis correction. Postoperative double eyelid ptosis improved. Since then, whenever the “cold” that has red and swollen pain, improved by antibiotic treatment. In 1979 due to corneal clouding led to blindness of the right eye, eyelid ptosis aggravated, with limb weakness, upper extremities as, and progressive increase, and can not engage in heavy manual labor. Past history, family history