Dentinogenesis imperfecta is a hereditary and developmental disturbance of the dentin which may be isolated or may occur in association with a number of syndromes. It is divided into three main types: type 1, type 2 and type 3. Type 1 Dentinogenesis imperfecta is always associated with osteogenesis imperfecta while type 2 and type 3 arises in isolated forms. watch the video here: https://youtu.be/itSoEXkzTtg Happy learning! #dentalmania | DentalManiak
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This is an extremely rare condition, do you know someone with Dentinogenisis Imperfecta? What is Dentinogenesis Imperfecta? It’s a genetic disorder that affects tooth development, specifically the dentin (the layer beneath the enamel). It leads to discolored, weak, and brittle teeth. ⸻ Key Features: • Discoloration: Teeth appear blue-gray or yellow-brown and may be translucent. • Weak dentin: Enamel chips off easily, exposing dentin, leading to rapid wear. • Brittle teeth: Prone to breaking, att
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