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先天性肌弛缓症在临床上较为少见,国内报道不多,现将我院所见1例报告如下。病历摘要吕姓,男孩,8个月,于1979年3月24日入院,因生后全身弛缓无力8个月而来就诊,至今仍不能抬头、抬腿,手臂亦不能上抬,手不能握物,哭无声,喉部经常有痰响,生后4个月时曾因发烧、气喘、苍白、发绀,诊断为“肺炎”,用抗菌素治疗好转。患儿常有憋气,近半月憋气加重,严重时面部、口唇发青,每次可达5分钟以上,经变换体位,拍背后才能缓解。生后未患过其他疾病,母乳喂养,未添加辅食,
Congenital achalasia is clinically rare, not many domestic reports, now see a hospital in our report as follows. Surgical record Abstract Surnamed Lu, boy, 8 months old, was admitted to hospital on March 24, 1979 and was treated for post-natal whole-body weakness for 8 months. She still can not look up, lift her leg, arm can not lift, her hand can not hold Objects, crying silently, the throat often sputum ring, 4 months after birth had a fever, asthma, pale, cyanosis, diagnosed as “pneumonia”, with antibiotic treatment improved. Frequent suffocation in children, nearly half of the increase in suffocation, severe facial, lips blue, each up to 5 minutes or more, by changing the position, after the beat can be alleviated. Not suffering from other diseases after birth, breastfeeding, no added food supplement,