Familial non-syndromic oligodontia

• Päätekijät: Seema Basoya (Tekijä), Sridevi Koduri (Tekijä), Ishita Gupta (Tekijä), Vinod Vijay Chandar (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: Wolters Kluwer Medknow Publications, 2015-01-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

Oligodontia, a rare genetic disorder, represents the congenital absence of more than six teeth in primary, permanent, or both dentitions and is usually the feature of a syndrome. Its occurrence as an isolated entity is even rarer. This article reports non-syndromic oligodontia in two siblings. One c...