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1982年12月6日收治1例萎缩性肌强直症,报告如下: 患者,男,33岁,3年前发现肢体活动不灵,常跌倒,双手无力,持物颤抖。用力咀嚼后不能立即张口,紧握拳后不能立即放松,用力屈臂不能立即伸直。上述症状发作频度和持续时间逐渐加重,每遇寒冷、精神紧张而加重。性功能减退,双眼视物模糊。患者母亲、哥哥、姐姐均患白内障,哥哥无生育能力,家族中无同类肌强直患者。患者面容瘦长,颧骨隆起,面肌、颞肌、咀嚼肌、前臂伸肌轻度萎缩。额
December 1, 1982 admitted to a case of atrophic myotonia, the report is as follows: The patient, male, 33 years old, three years ago found limb activity is not working, often falls, his hands weak, holding tremor. Can not be opened immediately after chewing hard, can not immediately relax after clenching the fist, forced flexor arm can not be immediately straightened. The frequency and duration of the above symptoms gradually aggravated, in each case of cold, mental stress and aggravate. Sexual dysfunction, binocular vision blurred. Patients mother, brother, sister are suffering from cataracts, brother no fertility, no other family members of myotonia patients. Patients face elongated, cheekbone bulge, facial muscles, temporal muscles, masticatory muscles, forearm extensor mild atrophy. amount