Ectodermal dysplasia: A retrospective evaluation of the clinical findings of forty-four cases in the 0-16 years age

IF 0.2 Q4 DENTISTRY, ORAL SURGERY & MEDICINE
Ebru Akleyin, Cansu Osmanoğulları Sarıyıldız, I. Yavuz, Özkan Adıgüzel
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Abstract

Aim: The aim of this study was to review the craniofacial anomaly results of children diagnosed with ectodermal dysplasia (ED) and to identify the oral requirements of ED cases. Methodology: The data of this study were obtained by taking clinical examinations and radiographs on forty-four (44) children (22 females and 22 males), 0-16 years aged, who were admitted to the Dicle University, Faculty of Dentistry due to dental problems and were diagnosed with ED. The number of affected siblings was ascertained, and systemic findings were evaluated. Malformations in the hair, nails, nose, skin, lips, and teeth were clinically examined. Results: The most common clinical findings were sparse hair, dry skin, sweating problems, respiratory difficulty, saddle nose, a history of fever, hearing loss, and deformation in the nails. In the intraoral and radiological examinations, findings were evaluated of conical teeth, protuberant lips, prosthetic rehabilitation, impacted teeth, and abnormal root resorption. The rates of ED in the siblings of the ED cases were determined as 39.2% in the siblings of male cases and 37.9% in the siblings of female cases. Conclusion: The frequency rates of the anomalies seen in ED obtained in this study can be considered important as a guide for further studies of individuals with ED. When multiple missing teeth and conical teeth are encountered, the dental practitioner should investigate whether or not there are other symptoms of ED, and it must not be forgotten that the dentist may be the first step in the diagnosis of this genetic irregularity.   How to cite this article: Akleyin E, Sarıyıldız Osmanoğulları C, Yavuz İ, Adıgüzel Ö. Ectodermal dysplasia: A retrospective evaluation of the clinical findings of forty-four cases in the 0-16 years age. Int Dent Res 2022;12(1):21-6. https://doi.org/10.5577/intdentres.2021.vol11.no1.4   Linguistic Revision: The English in this manuscript has been checked by at least two professional editors, both native speakers of English.
外胚层发育不良:回顾分析44例0 ~ 16岁儿童的临床表现
目的:本研究的目的是回顾诊断为外胚层发育不良(ED)的儿童颅面异常结果,并确定ED病例的口腔需求。方法:本研究的资料是通过对44(44)名儿童(22女22男)的临床检查和x线片获得的,年龄0-16岁,因牙齿问题被诊断为ED,并被Dicle大学牙科学院录取。确定受影响的兄弟姐妹数量,并评估系统表现。临床检查头发、指甲、鼻子、皮肤、嘴唇和牙齿的畸形。结果:最常见的临床表现为毛发稀疏、皮肤干燥、出汗、呼吸困难、鞍鼻、发热史、听力丧失和指甲变形。在口腔内和放射检查中,评估了锥形牙齿,突出的嘴唇,修复修复,阻生牙齿和牙根吸收异常的发现。男性患者的兄弟姐妹中ED发生率为39.2%,女性患者的兄弟姐妹中ED发生率为37.9%。结论:本研究获得的ED异常的频率可以作为ED个体进一步研究的重要指导。当遇到多颗缺牙和锥形牙时,牙科医生应该调查是否有ED的其他症状,不要忘记牙医可能是诊断这种遗传异常的第一步。如何引用本文:Akleyin E, Sarıyıldız Osmanoğulları C, Yavuz İ, Adıgüzel Ö。外胚层发育不良:回顾分析44例0 ~ 16岁儿童的临床表现。国际医学杂志,2016;12(1):21-6。https://doi.org/10.5577/intdentres.2021.vol11.no1.4语言修改:本手稿中的英语已由至少两名专业编辑检查,他们都是英语母语者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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