Prosthetic rehabilitation of a hypohidrotic ectodermal dysplasia patient: A case report
dc.authorid | 0000-0003-2684-0131 | en_US |
dc.authorid | 0000-0001-9575-7871 | en_US |
dc.authorid | 0000-0001-5466-7247 | en_US |
dc.contributor.author | Ayna, Emrah | |
dc.contributor.author | Gökçe, Dersim | |
dc.contributor.author | Polat, Zelal Seyfioğlu | |
dc.date.accessioned | 2022-09-28T13:00:55Z | |
dc.date.available | 2022-09-28T13:00:55Z | |
dc.date.issued | 2021 | en_US |
dc.department | Dicle Üniversitesi, Diş Hekimliği Fakültesi, Protetik Diş Tedavisi Bölümü | en_US |
dc.description.abstract | Aim: Ectodermal dysplasia is a rare hereditary disease that arises from a developmental disorder of 2 or more ectoderm-derived tissues. Ectodermal dysplasia is seen in 3 different types: anhidrotic, hypohidrotic, and hidrotic. Its anhidrotic and hypohidrotic types are the most common. This study presents the intraoral findings and dental treatment approach of a case diagnosed with hidrotic ectodermal dysplasia that demonstrates the typical characteristics of the disease, such as anodontia, hypohydrosis (reduced sweating), hypotrichosis (sparse hair), and loss of vertical dimension. Methodology: A 5-year-old male patient presented to the clinic of the Prosthetic Dental Treatment Department of the School of Dentistry at Dicle University on 25.10.2020 with complaint of missing teeth. A genetic analysis conducted in 2016 showed that he was a homozygous carrier of the p.Cys148Arg (c.442 T>C) mutation on the 5th exon of the ectodysplasin-A receptor (EDAR) gene. The mutation detected in the patient was associated with ectodermal dysplasia. An extraoral clinical examination revealed sparse hair, eyebrows, and eyelashes; soft, smooth, and dry skin; thin, linear wrinkles around the eyes and the lips; drooping, thickened lips; a sunken nose; fractured nails; hyperthermia due to lack of sweat glands; hyperkeratosis in the skin and soles of the feet; 2 nipples on one side of the chest; and reduced vertical facial height. An intraoral examination revealed anodontia; there were no teeth on the maxilla or the mandible and no radiographically identified tooth germ. Dry mouth due to a lack of sufficient saliva was another finding. Conclusion: In this case report, in the presence of anodontia, a removable total prosthesis, which is a non-invasive treatment option, was applied. Production of endosseous implants was postponed for a later time following the patient’s growth and development. | en_US |
dc.identifier.citation | Ayna, E., Gökçe, D. ve Polat, Z. S. (2021). Prosthetic rehabilitation of a hypohidrotic ectodermal dysplasia patient: A case report. International Dental Research, 11(Supplement 1), 292-298. | en_US |
dc.identifier.doi | 10.5577/intdentres.2021.vol11.suppl1.43 | |
dc.identifier.endpage | 298 | en_US |
dc.identifier.issn | 2146-1767 | |
dc.identifier.issue | Supplement 1 | en_US |
dc.identifier.startpage | 292 | en_US |
dc.identifier.trdizinid | 533268 | |
dc.identifier.uri | https://search.trdizin.gov.tr/yayin/detay/533268 | |
dc.identifier.uri | https://hdl.handle.net/11468/10581 | |
dc.identifier.uri | https://search.trdizin.gov.tr/yayin/detay/533268 | |
dc.identifier.volume | 11 | en_US |
dc.indekslendigikaynak | TR-Dizin | |
dc.institutionauthor | Ayna, Emrah | |
dc.institutionauthor | Gökçe, Dersim | |
dc.institutionauthor | Polat, Zelal Seyfioğlu | |
dc.language.iso | en | en_US |
dc.publisher | Uluslararası Diş Araştırmaları Birliği | en_US |
dc.relation.ispartof | International Dental Research | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Ectodermal dysplasia | en_US |
dc.subject | Anodontia | en_US |
dc.subject | Child | en_US |
dc.subject | Prosthetic treatment | en_US |
dc.title | Prosthetic rehabilitation of a hypohidrotic ectodermal dysplasia patient: A case report | en_US |
dc.title | Prosthetic rehabilitation of a hypohidrotic ectodermal dysplasia patient: A case report | |
dc.type | Article | en_US |
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