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营养不良性肌强直(Myotonic dystrophy)又叫萎缩性肌强直(Myotonic atrophica)。国外迭有报导,而国内则未见到,特将本院一例报告如下,供同道参考。病例告报王××、住院号53208、男性、32岁,已婚,技术员,湖南籍。自诉51年开始双上肢无力,消瘦,双手肌肉发硬,持物后不易放松,天冷情绪紧张可加重。56年后双下肢亦无力,变小,起坐开步须待片刻才能动作,说话,吞咽变慢。自后性欲减低,头髮腋毛阴毛减少,从不长胡子。易出汗,唾液多。60年在××院用过普罗卡因醯胺无效。于62年4月18日入我院。既往病史无特殊,家族中除妹妹有类似疾病外父母无此病。结婚10年未有小孩,否认有冶遊及性病史。
Malnutrition Myotonic dystrophy is also known as Myotonic atrophica. Foreign countries have repeatedly reported, but not seen in China, especially the case of a hospital report as follows, for fellow reference. Case report Wang XX, hospital number 53208, male, 32 years old, married, technician, Hunan nationality. Prosecutors 51 years since the upper limb weakness, weight loss, hands and muscles hard, difficult to relax after holding things, cold weather can aggravate tension. 56 years later both lower extremities also weakness, smaller, sit-up to be a moment to be action, speak, swallow slowly. Since the reduction of libido, hair armpit hair pubic hair reduced, never long beard. Easy to sweat, saliva and more. 60 years in × × hospital used procaine amine invalid. On April 18, 62 into our hospital. There is no history of past illness, the family except the sister has a similar disease without the disease outside the parents. Married 10 years without children, denied a history of smelting and sexually transmitted diseases.