Heterogeneity of Orofacial Clefts and Associated Anomalies in China

被引:1
作者
Jiang, Leheng [1 ]
Jiang, Chanyuan [1 ]
Wang, Yongqian [1 ]
Song, Tao [1 ]
Yin, Ningbei [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Plast Surg Hosp, Dept Cleft Lip & Palate, 33 Badachu Rd, Beijing 100144, Peoples R China
关键词
Cleft lip and palate; congenital malformations; microform cleft lip; ORAL CLEFTS; LIP; PALATE; INFANTS; BIRTH; SPECTRUM;
D O I
10.1097/SCS.0000000000009611
中图分类号
R61 [外科手术学];
学科分类号
摘要
Despite the large number of affected individuals in China, information on the descriptive epidemiology of orofacial clefts in the Chinese population remains limited. Therefore, the authors aimed to report a detailed clinical classification of orofacial clefts, including microform cleft lip (CL), and associated malformations in patients from a major cleft surgical unit in China. The authors reviewed the medical records of 718 patients who underwent primary cleft repair surgery at their center between December 2016 and April 2023. The sex distribution varied with cleft type and extent, and males had a higher proportion of clefts with increased severity than females. In patients with a unilateral CL, the ratio of left-to-right-sided clefts was 1.85:1. The frequency of associated congenital malformations in patients with microform CL only, overt CL only, CL and palate, and cleft palate only was 8.0%, 7.6%, 14.9%, and 30.9%, respectively. A total of 98 malformations were observed in 69 patients with congenital anomalies of unknown origin. Among these, cardiovascular anomalies were the most common, identified in 27 patients (39.1%), followed by head and neck and musculoskeletal anomalies. The high risk of heart defects highlights the importance of routine echocardiography. Microform CL exhibited increased prevalence and a similar frequency of associated malformations with overt CL, suggesting that this mild phenotype requires further attention by clinicians.
引用
收藏
页码:E698 / E701
页数:4
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