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永恒动脉干并室间隔缺如、房间隔缺损,临床较少见。我院遇到一例,并经尸检证实。患儿男,9个月。因阵发性哭闹伴频繁呕吐1天,于1982年1日2日入院。患儿为第一胎,足月顺产。生后无紫绀。3月前因咳喘、发绀诊为支气管肺炎,住院10天治愈。查体:体温39.2℃,脉搏166。发育、营养中等.神清,面色青灰,唇稍绀。皮肤、粘膜无黄
Eternal arterial and interventricular septal defect, atrial septal defect, clinical less common. A case of our hospital, and confirmed by autopsy. Children male, 9 months. Due to paroxysmal crying with frequent vomiting 1 day, on January 1, 1982 admission. Children for the first child, full-term birth. No cyanosis after birth. 3 months ago due to cough, cyanosis clinically diagnosed as bronchial pneumonia, hospitalized 10 days to cure. Physical examination: body temperature 39.2 ℃, pulse 166. Development, nutrition medium. God clear, looking gray, slightly cyanotic lips. Skin, mucous membrane without yellow