Abstract：
OBJECTIVE: Macrostomia, or lateral cleft lip, which is known as Tessier cleft type 7, is one of the rarest facial anomalies. The purpose of this review is to describe the main characteristics, epidemiology, aetiology and treatment of this anomaly.
METHODS: We present an overview of surgical techniques as well as a review of all 36 cases of bilateral asyndromic macrostomia reported to this da in the literature. Furthermore, we report the case of a 4-month male infant with bilateral transverse cleft lip and analyse the treatment decision and the procedure itself.
CONCLUSIONS: Early diagnosis and surgical intervention are crucial in treating children with these malformations. Adequate timely reconstruction plays a main role in both physical and psychological rehabilitation.
METHODS: We present an overview of surgical techniques as well as a review of all 36 cases of bilateral asyndromic macrostomia reported to this da in the literature. Furthermore, we report the case of a 4-month male infant with bilateral transverse cleft lip and analyse the treatment decision and the procedure itself.
CONCLUSIONS: Early diagnosis and surgical intervention are crucial in treating children with these malformations. Adequate timely reconstruction plays a main role in both physical and psychological rehabilitation.
摘要：
目标：大口，或者侧唇裂，被称为Tessier裂隙7型，是最罕见的面部异常之一。这篇综述的目的是描述主要特征，流行病学,这种异常的病因和治疗。
方法：我们对手术技术进行了概述，并对文献中报道的所有36例双侧无性巨大口炎进行了综述。此外，我们报告了一个4个月的男性婴儿双侧横向唇裂的病例，并分析了治疗决定和手术本身。
结论：早期诊断和手术干预对于治疗这些畸形的儿童至关重要。充分及时的重建在身心康复中起着主要作用。
方法：我们对手术技术进行了概述，并对文献中报道的所有36例双侧无性巨大口炎进行了综述。
结论：早期诊断和手术干预对于治疗这些畸形的儿童至关重要。
