Autor: |
Dogra, Gagan, Pannu, Parampreet, Singh, Neeru |
Předmět: |
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Zdroj: |
Indian Journal of Dental Sciences; Sep2010, Vol. 2 Issue 4, p36-38, 3p, 6 Black and White Photographs |
Abstrakt: |
Crouzon syndrome is a rare genetic disorder, characterized by both the systemic and oral manifestations. The syndrome manifests as craniosynostosis, optic atrophy, exopthalmos, nystagmus, hypertelorism and pssittichoronia. Hypoplastic maxilla with high arched palatal vault, crowding of teeth, hypodontia, anterior and posterior crossbite are few of the oral manifestations. A case report of a child suffering from Crouzon syndrome along with the associated oral manifestations and its management is being presented. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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