Case Report A states in the case of ectodermal dysplasia that such ab The purpose of this article is to describe a literature review AuthorsYear ReportedGenderAgeInvolved DentitionHEDRemark Sarnat e ID: 961019
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Pediatric Dentistry Ð 22:1, 2000American Academy of Pediatric Dentistry 49 Case Report A states in the case of ectodermal dysplasia that such ab- The purpose of this article is to describe a literature review AuthorsYear ReportedGenderAgeInvolved DentitionHEDRemark Sarnat et al.1953M6y~16yprimary & permanentaccompanied Eisenson1956M5yprimary & permanentaccompanied Ochia
i et al.1961M4y 8 moprimary & permanentaccompanied Issa Herman et al.1977F14ypermanentaccompanied1980F14ypermanentaccompaniedsame case with Herman Yamashita et al.1992F8ypermanentnot accompanied Table 1. List of Reported Cases of Anodontia Pediatric Dentistry Ð 22:1, 2000American Academy of Pediatric Dentistry 51 To our regret, she did not return to our clinic after 6 Am
ong them, X-linkedclefting syndrome, Rapp-Hodgkin syndrome, and Ellis-van The gene responsible for the X-linked type has been recentlyX-linked form and recessive form through genetic testing. Since have stated that an autosomal recessive mode of in- Anodontia can be diagnosed by taking a panoramic radio- The dental literature describes the dental treatment and suggest that
an initial prosthesis should be delivered Fig 4. Intraoral photograph with insertion of the acrylic full dentures. Fig 3. Cephalometric radiograph taken at 5 years and 3 months of age. Fig 5. Frontal view beforeinserting the full dentures. Fig 6. Frontal view afterinserting the full dentures.Her facial appearance wasimproved due to alteration ofthe lower facial patterns