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International journal of clinical pediatric dentistry · 2019

Management of Dentinogenesis Imperfecta: A Report of Two Cases.

Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Kaur Avninder, Kumar Sanchit, Karda Babita, Chibh Richa

Аннотация

UNLABELLED: Dentinogenesis imperfect is a hereditary dentin defect leading to discoloration as well as early tooth wear. Timely diagnosis and treatment are required to prevent further tooth loss. Two patients reported to the department of pediatrics dentistry with dentinogenesis imperfecta (DI). In the first case, patient complained of discoloration of both primary and permanent teeth and delayed eruption of permanent teeth. In the second case report, patient reported with mobile anterior tooth and missing teeth due to extraction of mobile teeth. Extraction was followed by space maintainers in the first case, and extraction was followed by partial denture in the second case. Both the patients and their parents were happy with the treatment provided.

HOW TO CITE THIS ARTICLE: Kaur A, Kumar S, Karda B, et al. Management of Dentinogenesis Imperfecta: A Report of Two Cases. Int J Clin Pediatr Dent 2019;12(5):464-466.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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