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本院收治1例先天性双侧面横裂合并唇裂,腭裂、牙槽突裂、上颌骨裂及先天性睑球结膜粘连的患者,并给予手术治疗,效果尚好。此种畸形属面颌部胚胎性多突起联合不全所致,国内文献未见报道。兹将病例报告如下: 患者聂××,男,4周岁。住院号241076。因该患儿出生时即发现两侧面部裂开,上唇裂开、腭部裂开,吸吮困难,流口水,睑球结膜粘连,影响美观,要求修补,于1986年3月25日入院。据患儿母亲叙述,
The hospital admitted a case of congenital bilateral transverse transverse cleft lip, cleft palate, alveolar cleft, maxillary fissure and congenital symblepharon adhesion patients, and given surgical treatment, the effect is still good. This deformity is the surface of the Ministry of Jaw embryo multiple prominence due to incomplete, the domestic literature has not been reported. The case report is as follows: Patient Nie × ×, male, 4 years of age. Hospital number 241076. Because of the child was born on both sides of the face that was found on the split, upper lip split, cleft palate, sucking difficulties, drooling, bulbar conjunctival adhesions, affecting the appearance, requiring repair, in March 25, 1986 admission. According to the description of children's mother,