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

dc.authorid0000-0003-4302-6561en_US
dc.authorid0000-0001-6953-747Xen_US
dc.authorid0000-0001-6089-3013en_US
dc.contributor.authorAkleyin, Ebru
dc.contributor.authorSarıyıldız, Cansu Osmanoğulları
dc.contributor.authorYavuz, İzzet
dc.contributor.authorAdıgüzel, Özkan
dc.date.accessioned2022-10-27T08:00:19Z
dc.date.available2022-10-27T08:00:19Z
dc.date.issued2022en_US
dc.departmentDicle Üniversitesi, Diş Hekimliği Fakültesi, Çocuk Diş Hekimliği Bölümüen_US
dc.description.abstractAim: 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.en_US
dc.identifier.citationAkleyin, E., Sarıyıldız, C. O., Yavuz, İ. ve Adıgüzel, Ö. (2022). Ectodermal dysplasia: A retrospective evaluation of the clinical findings of forty-four cases in the 0-16 years age. International Dental Research, 12(1), 21-26.en_US
dc.identifier.doi10.5577/intdentres.2022.vol12.no1.4
dc.identifier.endpage26en_US
dc.identifier.issn2146-1767
dc.identifier.issue1en_US
dc.identifier.startpage21en_US
dc.identifier.trdizinid1123961
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/1123961
dc.identifier.urihttps://hdl.handle.net/11468/10706
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/1123961
dc.identifier.volume12en_US
dc.indekslendigikaynakTR-Dizin
dc.institutionauthorAkleyin, Ebru
dc.institutionauthorAdıgüzel, Özkan
dc.language.isoenen_US
dc.publisherUluslararası Diş Araştırmaları Birliğien_US
dc.relation.ispartofInternational Dental Research
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectEctodermal dysplasiaen_US
dc.subjectMalformationen_US
dc.subjectConical toothen_US
dc.subjectSparse hairen_US
dc.titleEctodermal dysplasia: A retrospective evaluation of the clinical findings of forty-four cases in the 0-16 years ageen_US
dc.titleEctodermal dysplasia: A retrospective evaluation of the clinical findings of forty-four cases in the 0-16 years age
dc.typeArticleen_US

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