Ectodermal dysplasia: a rare entity featuring complete anodontia: Case report and review of literature with a note on genetics

dc.contributor.authorKamath, Jasmine Shanthi
dc.contributor.authorKini, Raghavendra
dc.contributor.authorNaik, Vathsala
dc.date.accessioned2018-11-23T06:48:44Z
dc.date.available2018-11-23T06:48:44Z
dc.date.issued2017
dc.departmentİnönü Üniversitesien_US
dc.descriptionJ Turgut Ozal Med Cent 2017;24(3):342-4.en_US
dc.description.abstractAbstract Ectodermal dysplasias are a large, multifarious group of inherited disorders, characterized by a flaw in the tissues derived from the embryonic ectoderm. The incidence of ectodermal dysplasia is rare. Various alterations in the genes coding for proteins like EDA, EDAR, EDARADD are the causes for the manifestations of ectodermal dysplasia. Oligodontia or hypodontia of the deciduous and/ or permanent dentition is the most common intra-oral finding. Ectodermal dysplasia is not only physically devastating to the patients but also emotionally demoralizing. It is essential that they be treated at an early age to improve their quality of life. The following case report aims at describing the condition in a patient with complete anodontia and discusses the genetic component of the disorder. Oral rehabilitation was achieved by using removable prosthesis. Keywords: Ectodermal Dysplasia; EDA; EDAR; EDARADD; Anodontia.en_US
dc.identifier.citationJasmine Shanthi K., Raghavendra K., Vathsala N. Ectodermal dysplasia: a rare entity featuring complete anodontia: Case report and review of literature with a note on genetics. J Turgut Ozal Med Cent 2017;24(3):342-4.en_US
dc.identifier.doi10.5455/jtomc.2017.02.025en_US
dc.identifier.endpage344en_US
dc.identifier.issue3en_US
dc.identifier.startpage342en_US
dc.identifier.urihttp://www.totmdergisi.org/articles/2017/volume24/issue3/2017_24_3_23.pdf
dc.identifier.urihttps://hdl.handle.net/11616/9188
dc.identifier.volume24en_US
dc.language.isoenen_US
dc.publisherTurgut Özal Tıp Merkezi Dergisien_US
dc.relation.ispartofTurgut Özal Tıp Merkezi Dergisien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectEctodermal Dysplasiaen_US
dc.subjectEDAen_US
dc.subjectEDARen_US
dc.subjectEDARADDen_US
dc.subjectAnodontiaen_US
dc.titleEctodermal dysplasia: a rare entity featuring complete anodontia: Case report and review of literature with a note on geneticsen_US
dc.typeArticleen_US

Dosyalar

Orijinal paket
Listeleniyor 1 - 1 / 1
Yükleniyor...
Küçük Resim
İsim:
2017_24_3_23.pdf
Boyut:
653.64 KB
Biçim:
Adobe Portable Document Format
Açıklama:
Makale Dosyası
Lisans paketi
Listeleniyor 1 - 1 / 1
Küçük Resim Yok
İsim:
license.txt
Boyut:
1.71 KB
Biçim:
Item-specific license agreed upon to submission
Açıklama: