| Autor: |
SANKAR, A. J. SAI, SAMATHA, Y., SUNEELA, S., BABU, D. ANKINEEDU |
| Předmět: |
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| Zdroj: |
Journal of Clinical & Diagnostic Research; Jan2014, Vol. 8 Issue 1, p282-284, 3p |
| Abstrakt: |
Amelogenesis Imperfecta (AI) is a hereditary enamel defect which is characterized by developmental abnormalities in the quantity and/ or quality of enamel. This condition has been associated with dental anomalies, including taurodontism, congenitally missing teeth, delayed eruption, crown resorption, pulpal calcifications and odontogenic fibromas. This paper presents two cases of AI which were associated with multiple impacted permanent teeth in both the cases; and pulpal calcifications and pericoronal odontogenic fibromas of W.H.O type additionally, in one of the cases. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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