Dentin dysplasia type II: An exclusive report of two cases in siblings

• Príomhchruthaitheoirí: Deepak Daryani (Údar), Gopakumar R Nair (Údar), Giridhar Naidu (Údar)
• Formáid: LEABHAR
• Foilsithe / Cruthaithe: Wolters Kluwer Medknow Publications, 2017-01-01T00:00:00Z.
• Ábhair: article
• Rochtain ar líne: Connect to this object online.

Dentin dysplasia is a rare autosomal dominant disorder affecting dentin and resulting in early loss of teeth. Although dentin dysplasia type I is reported to have an incidence of 1 in 100,000, dentin dysplasia type II is considered to be an extremely rare genetic disorder, the prevalence of which is...