Slah-Ud-Din Saad, Ali Kunza, Mahd Syed Muhammad, Nisar Samaha, Nisar Omar
Internal Medicine, Shalamar Medical & Dental College, Lahore, PAK.
Cureus. 2023 Jul 10;15(7):e41641. doi: 10.7759/cureus.41641. eCollection 2023 Jul.
Background Facial anomalies comprise a significant component of birth defects, with oral clefts being the second most common entity in this group. All organ systems within the body can be affected by congenital anomalies, mostly affecting the musculoskeletal system. Birth defects are among the leading causes of infant mortality and morbidity around the world. Objectives To find the factors associated with an increased risk of facial malformations so that steps for improving preventive measures can be taken. Methodology This was a cross-sectional study in which the data were collected from the files of infants admitted to the pediatric department. Data regarding the type of congenital anomaly, maternal investigations done during pregnancy, maternal history of medication, diabetes, hypertension, radiation exposure, smoking, and alcohol history, and family history of congenital anomalies was collected from the files of neonates and from the pediatrician. In the case of unanswered questions, the parent was contacted after 10 days with their consent. Results Of the sample size of 259 children (males: 132; females: 127), 68 (26%) had a cleft lip, 69 (27%) had a cleft palate, 110 (42%) had both cleft lip and palate, five (2%) had a cleft lip with nasal deformity, five (2%) had a cleft lip and palate with nasal deformity, and two (1%) had hypertelorism. Eight percent of neonates with craniofacial malformations had a family history of congenital malformations; 80.7% of neonates had a history of parental consanguinity; and 19.3% were unrelated. In regard to the mothers, 41.3% of the mothers had diabetes, 4% had hypertension, 4% had both gestational diabetes and hypertension, and 55% had neither of these diseases. Of the 55% of mothers with neither disease, 75% were married to their cousins, while 25% were not married within the family. Practical implications This study, highlighting the major factors contributing to the incidence of congenital facial malformations, will educate the community and establish awareness among the younger generation of the top causes of anomalies, therefore making a huge impact on increasing efforts to reduce the prevalence of congenital anomalies. Conclusion Defects of both the cleft lip and palate had the highest prevalence of facial malformations among study subjects (110 patients (42%)). Parental consanguinity is one of the leading factors associated with an increased risk of facial malformations.
背景 面部畸形是出生缺陷的重要组成部分,唇腭裂是该组中第二常见的病症。体内所有器官系统都可能受到先天性异常的影响,其中大多数影响肌肉骨骼系统。出生缺陷是全球婴儿死亡和发病的主要原因之一。目的 找出与面部畸形风险增加相关的因素,以便采取措施改进预防措施。方法 这是一项横断面研究,数据从儿科收治的婴儿病历中收集。从新生儿病历和儿科医生处收集有关先天性异常类型、孕期母亲检查情况、母亲用药史、糖尿病、高血压、辐射暴露、吸烟和饮酒史以及先天性异常家族史的数据。对于未回答的问题,经家长同意后在10天后与其联系。结果 在259名儿童样本(男132名;女127名)中,68名(26%)有唇裂,69名(27%)有腭裂,110名(42%)既有唇裂又有腭裂,5名(2%)有唇裂伴鼻畸形,5名(2%)有唇腭裂伴鼻畸形,2名(1%)有眼距过宽。8%有颅面畸形的新生儿有先天性畸形家族史;80.7%的新生儿有父母近亲结婚史;19.3%无血缘关系。关于母亲,41.3%的母亲患有糖尿病,4%患有高血压,4%同时患有妊娠期糖尿病和高血压,55%无上述两种疾病。在无上述两种疾病的55%母亲中,75%与表亲结婚,25%非家族内通婚。实际意义 本研究突出了导致先天性面部畸形发生率的主要因素,将对社区进行教育,并在年轻一代中树立对异常主要原因的认识,从而对加大减少先天性异常患病率的努力产生巨大影响。结论 在研究对象中,唇腭裂畸形在面部畸形中患病率最高(110例患者,42%)。父母近亲结婚是与面部畸形风险增加相关的主要因素之一。