Abstract: Hypodontia, together with other characteristics similar in each of three sisters, established a diagnosis of anhidrotic ectodermal dysplasia. The clinical features of the patients are described, and the oral and dental manifestations are presented. The parents were found to be free of all the aberrant conditions described in the proband.
Publication Year: 1972
Publication Date: 1972-05-01
Language: en
Type: article
Indexed In: ['crossref', 'pubmed']
Access and Citation
Cited By Count: 17
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