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The relationship of amelogenesis imperfecta and nephrocalcinosis syndrome

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dc.creator KIRZIOĞLU, Zühal
dc.creator Sezer, M. Tugrul
dc.creator Yuksel, Seref
dc.creator Ulu, K. Gorkem
dc.date 2009-10-31T22:00:00Z
dc.date.accessioned 2020-10-06T10:50:09Z
dc.date.available 2020-10-06T10:50:09Z
dc.identifier 9c4c50da-b8d0-43c8-8954-812cbeab3e53
dc.identifier 10.4317/medoral.14.e579
dc.identifier https://avesis.sdu.edu.tr/publication/details/9c4c50da-b8d0-43c8-8954-812cbeab3e53/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/67473
dc.description Aim: To analyze the prevalence and associated oral findings of nephrocalcinosis in a group of patients affected with amelogenesis imperfecta (AI). The relationship between types of AI and nephrocalcinosis were also evaluated. Design: This study examines patients who were referred to Pediatric Dentistry Department of SDU between the years of 2002-2007 and who, upon clinical and radiological examination, were diagnosed with AI and treated. Patients were offered information about the possibility of nephrocalcinosis syndrome. Patients who agreed to have tests carried out on their renal system were advised to visit the department of nephrology at the clinic. Results: Suspicious radiopacity was observed during renal ultrasonography of a controlled number of patients with hypoplastic type AI. Laboratory results revealed low Ca values (100-300 mg/days) and normal P values (0.4-1.3 g/days). Delayed eruption, gingival hyperplasia, pulp stones and orthodontic problems were also observed in the same patient groups. Conclusion: Although renal findings were observed in a few patients, pediatric dentists are the doctors who are the first to have early contact with this patient group. Because of the potential risk of nephrocalcinosis, early diagnosis may offer good prognosis.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title The relationship of amelogenesis imperfecta and nephrocalcinosis syndrome
dc.type info:eu-repo/semantics/article


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