Florid cemento osseous dysplasia and dentygerous cyst in a patient with apert syndrome: A case report
Apert syndrome is a rare congenital malformation characterized by craniocinocytosis, craniofacial anomalies and symmetric syndactyly of the feet and hands. Oral manifestations of Apert syndrome usually represents bifid uvula, malposition of the teeth, severe open bite, tooth decay and periodontal di...
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Aineistotyyppi: | Kirja |
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Selçuk University,
2019-11-01T00:00:00Z.
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A1234.567 |
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Nide 1 | Saatavissa |