Document Details

Document Type : Article In Journal 
Document Title :
Hereditary Hypohidrotic Ectodermal Dysplasia With Anodontia: A Case Report
Hereditary Hypohidrotic Ectodermal Dysplasia With Anodontia: A Case Report
 
Document Language : English 
Abstract : A four-year-old Saudi boy presented, for the first time, with the characteristic clinical features of hypohidrotic ectodermal dysplasia. Intraoral examination revealed total anodontia of the deciduous teeth. Roentgenographic examination showed four cone-shaped crowns with incomplete roots in bony crypts consistent with permanent canines. No other calcification of the permanent successors was noted. The child was the only member of his family who suffered from hypohidrotic ectodermal dysplasia. 
ISSN : 0 
Journal Name : SDJ 
Volume : 6 
Issue Number : 1 
Publishing Year : 1994 AH
1994 AD 
Article Type : Article 
Added Date : Thursday, February 18, 2010 

Researchers

Researcher Name (Arabic)Researcher Name (English)Researcher TypeDr GradeEmail
رباب فتيحFeteih, Rabab ResearcherDoctorate 

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