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先天性面斜裂较三面横裂,正中裂等更为少见。现把我科于1973年收治一例报告于下。病例报告患儿,女性、10岁。因面颌部先天性畸形要求整形治疗,于1973年11月19日入院。患儿为第一胎,足月、顺产,家族中无同样病史。检查:患儿神志清楚,发育及营养较差,合作欠佳,心律齐92次/分,未及杂音,肺听诊(一),腹软,肝脾未及,血压100/60毫米汞柱。面颌部检查:右侧下眼睑裂开呈“V”字形,外翻,有索条状组织和球结膜相连,未见泪点。裂隙下方有一0.6×0.5毫米之圆孔和上
Congenital facial spur more than three transverse, median fissure more rare. Now my section in 1973 admitted a report on the next. Case report Children, female, 10 years old. Due to facial congenital malformations requiring plastic surgery, was admitted to hospital on November 19, 1973. Children with the first child, full-term, spontaneous abortion, no similar family history. Check: children with clear mind, poor development and nutrition, poor cooperation, heart rate Qiqiun / min, no noise, pulmonary auscultation (a), abdominal soft, liver and spleen not yet, blood pressure 100/60 mm Hg. Facial jaw examination: the lower eyelid dehiscence was “V” shape, eversion, a strip of tissue and the conjunctiva connected, no tears. Below the fissure there is a 0.6 × 0.5 mm round hole and up