Noordhoff M S, Cheng W S
Ann Plast Surg. 1982 Jan;8(1):83-92. doi: 10.1097/00000637-198201000-00013.
Eight patients, aged 9 months to 9 years, each with unusual complete cleft of the primary and secondary palate on one side and a complete cleft of the secondary palate on the opposite side, were evaluated. All showed varying deficiencies of median facial mesodermal dysgenesis characterized by absent frenulum, indefinite cupid's bow, deficient septal cartilage and nasal spine, and absent central and lateral incisor of the cleft side of the premaxilla. Computerized tomographic scan confirmed the absence of the central nervous system anomalies seen in midline clefts. Cephalometric studies revealed maxillary hypoplasia and no evident hypotelorism. These patients demonstrate a definable lack of median mesodermal penetration along with failure of lateral mesodermal penetration. It is to be noted that median facial dysgenesis can occur without recognizable central nervous system disorders. It is quite possible that microforms of median facial dysgenesis occur in unilateral and bilateral cleft lip and palate patients. This would help explain the wide variations of clefting seen clinically.
对8例年龄在9个月至9岁之间的患者进行了评估,这些患者一侧为原发性和继发性腭裂的罕见完全性腭裂,另一侧为继发性腭裂的完全性腭裂。所有患者均表现出不同程度的面中部中胚层发育不全,其特征为系带缺失、唇弓不明确、鼻中隔软骨和鼻棘缺损,以及上颌前部腭裂侧的中切牙和侧切牙缺失。计算机断层扫描证实不存在中线腭裂中所见的中枢神经系统异常。头影测量研究显示上颌发育不全,且无明显的眼距过窄。这些患者表现出可明确的面中部中胚层穿透不足以及外侧中胚层穿透失败。需要注意的是,面中部发育不全可在无明显中枢神经系统疾病的情况下发生。很有可能在单侧和双侧唇腭裂患者中出现面中部发育不全的微小型。这将有助于解释临床上所见腭裂的广泛差异。