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Dentin dysplasia type I--a case report.

F Neumann¹, F Würfel, T Mundt

¹Department of Oral and Maxillofacial Surgery/Plastic Operations, Ernst Moritz Arndt University, Greifswald, Germany.

Annals of Anatomy = Anatomischer Anzeiger : Official Organ of the Anatomische Gesellschaft

|March 19, 1999

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Dentin dysplasia type I is a rare genetic disorder affecting teeth. Treatment involves tooth extraction, cyst removal, sinus surgery, and denture placement for restoration.

Area of Science:

Dentistry
Genetics
Oral Pathology

Background:

Dentin dysplasia type I is a rare autosomal dominant genetic disorder.
It affects both primary and permanent dentition, presenting unique clinical challenges.

Observation:

The case report details clinical and histological findings of dentin dysplasia type I.
Radiographic evidence includes X-ray and CT scans revealing characteristic dental anomalies.

Findings:

Treatment necessitated extraction of all affected teeth.
Surgical interventions included ectomization of cystic alterations and paranasal sinus revision.

Implications:

Successful aesthetic and functional rehabilitation was achieved through complete denture insertion.

Related Experiment Videos

This case highlights a comprehensive management approach for dentin dysplasia type I.