المستخلص: |
Oligodontia is defined as agenesis of six or more teeth excluding the third molars. It is a rare finding which has not been frequently documented. Most often oligodontia appears as a part of some congenital syndromes as hereditary ectodermal dysplasia, . The consequences of missing teeth include affected masticatory function, abnormal occlusion, altered facial appearance which can cause psychological distress in some patients. The present article reports a rare case of non-syndromic oligodontia in a 5 year old boy patient. The child was assessed clinically and radiographically. Orthopantomographic examination revealed agenesis of six permanent teeth excluding the third molars and two primary teeth. Detailed examination revealed that the agenesis of teeth was not associated with any syndromes or systemic disorders. The parents were educated about probable future treatment options for their growing child. Management of oligodontia generally requires a multidisciplinary approach. It includes various restorative, orthodontic and prosthodontic procedures to improve the esthetics and function.
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