Hipoplastik Tip Amelogenezis İmperfektalı

Yıl 2012, Cilt: 6 Sayı: 2, 1181 - 1186, 01.07.2012

Canan Akay Banu Çukurluöz Suat Yaluğ

Öz

Amelogenesis imperfecta is a hereditary disorder that affects the formation of the dental enamel both in the primary and permanent dentition. Many cases are inherited, either as autosomal dominant, autosomal recessive or as an X-linked trait. This article presents an adult patient suffering from amelogenesis imperfecta who successfully overcame the esthetic, functional, phonetic and psychosocial problems by receiving prosthetic rehabilitation

Anahtar Kelimeler

Amelogenesis imperfecta, hypoplastic type

Hastanın Protetik Rehabilitasyonu

Öz

Amelogenezis imperfekta, mine oluşumunu etkileyen, süt ve daimi dentisyonda gözlenen herediter bir hastalıktır. Birçok vakada otozomal dominant, otozomal resesif ya da X kromozomuna bağlı genetik geçiş gösterir. Bu makalede erişkin dönemde kliniğimize başvurmuş amelogenezis imperfektalı bir hastanın protetik rehabilitasyonu sonucu estetik, fonksiyon, fonasyon ve psikososyal problemlerinin başarılı şekilde ortadan kaldırıldığı bir olgu raporu sunulmaktadır

Anahtar Kelimeler

Amelogenezis imperfekta, hipoplastik tip

Kaynakça

• Ergeneli S., Yılmaz S., Sandallı N. Amelogenezis imperfecta ve nefrokalsinozis sendromu. 7Tepe Klinik 1: 7-11, 2005.
• Bharath Y., Shetty A. Oral rehabilitation of a young adult with amelogenesis imperfecta: A clinical report. J. Indian Prosthodont. Soc. 10: 240-245, 2010.
• Robinson FG., Haubenreich JE. Oral rehabilitation of a young adult with hypoplastic amelogenesis imperfecta: A clinical report. J. Prosthet. Dent. 95: 10-13, 2006.
• Enginas RP., Espona IG., Montela JM. Amelogenesis imperfecta, diagnosis and resolution of a case with hypoplasia and hypocalcification of enamel, dental agenesis, and skeletal open bite. Quintessence Int. 32: 183-189, 2001.
• Finn SB. Clinical Pedodontics, 4th ed. Philadelphia: W.B. Saunders, 1973.
• Backman B., Holm AK. Amelogenesis imperfecta: prevalence and incidence in a northern Swedish country. Community Dentistry Oral Epidemiology 14: 43-47, 1986.
• Witkop CJ., Sauk JR. J. Heritable defects of enamel. In: Stewart RE., Prescott GH., editors. Oral facial genetics. St Louis: C.W. Mosby Co; 1976, p.151-226
• Altuğ-Ataç AT, Erdem D. Prevalence and distribution of dental anomalies in orthodontic patients. Am. J. Orthod. Dentofacial Orthop. 131: 510-514, 2007.
• Sedano HO. Congenital oral anomalies in Argentinian children. Community Dent. Oral Epidemiol. 3: 61-63, 1975.
• Chosack A., Eidelman E., Wisotski I., Cohen T. Amelogenesis imperfecta among Israeli Jews and the description of a new type of local hypoplastic autosomal recessive amelogenesis imperfecta. Oral Surg. Med. Oral Pathol. 47: 148-156, 1979.
• Canger EM., Çelenk P., Yenisey M., Odyakmaz S.Z. Amelogenesis imperfecta, hypoplastic type associated with some dental abnormalities: A case report. Braz. Dent. J. 21: 170-174, 2010.
• Gisler V., Enkling N., Zix J., et al. A multidisciplinary approach to the functional and esthetic rehabilitation of amelogenesis imperfecta and open bite deformity: a case report. J. Esthet. Restor. Dent. 22: 282-296, 2010.
• Ayers KM., Drummond BK., Harding WJ., et al. Amelogenesis imperfecta-multidisciplinary management from eruption to adulthood. Review and case report. NZ Dent. J. 100:101-104, 2004.
• Aldred M., Savarirayan R., Crawford P. Amelogenesis imperfecta: a classification and catalogue for the 21st century. Oral Diseases 9: 19–23, 2003.
• Crawford P., Aldred M., Zupan AB. Amelogenesis imperfecta: Orphanet J. Rare Dis. 2: 17, 2007.
• Chamarthi V., Varma BR., Jayanthi M. Amelogenesis imperfecta: A clinician’s challenge. Journal of Indian Society of Pedodontics and Preventive Dentistry 1: 70-73, 2012.
• Ayna B., Ayna E., Hamamcı N., et al. Amelogenezis imperfektalı iki hastada estetik ve fonksiyonun sağlanması: Olgu sunumu. Cumhuriyet Üniversitesi Diş Hekimliği Fakültesi Dergisi 11: 113-117, 2008.
• Dellow EM., Harley KE., Unwin RJ., et al. Amelogenesis Imperfecta, nephrocalcinosis and hypocalciuria sydrom in two siblings from a large family with consanguineous parents. Nephrol. Dial. Transplant. 13: 193-196, 1998.
• Schossig A., Wolf N., Kapferer I., et al. Epileptic encephalopathy and amelogenesis imperfecta: Kohlschütter-Tönz syndrome. European Journal of Medical Genetics 55: 319-322, 2012.
• Ooya K., Nalbandian J., Noikura T. Autosomal recessive rough hypoplastic amelogenesis imperfecta. Oral Surg. Oral Med. Oral Pathol. 65: 449-458, 1988.
• Akkocaoğlu M., Kasapoğlu O., Çağırankaya B. Amelogenesis imperfecta with supernumerary and unerupted teeth: A case report. Hacettepe Diş Hekimliği Dergisi 28: 46-51, 2004.
• Koyutürk AE., Kahvecioğlu F., Şener Y., et al. Geçici Overdenture protezler ile rehabilite edilen amelogenesis imperfecta: Olgu sunumu. Cumhuriyet Üniversitesi Diş Hekimliği Dergisi 9: 41-45, 2006.
• Tümen E. Amelogenezis imperfacta: sınıflaması, klinik teşhisi ve tedavi yaklaşımları (Derleme). Dicle Diş Hekimliği Dergisi 10: 58-62, 2009.
• Sundell S. Hereditary amelogenesis imperfecta. Swed. Dent. J. 10: 151-63, 1986.
• Çakmak T., Ateş SM., Altıntaş SH., et al. Amelogenesiz imperfectalı bir hastanın overlay protezle rehabilitasyonu: olgu sunumu. SÜ. Diş Hekimliği Fakültesi Dergisi 20: 140-143, 2011.
• Sarı T., Üsümez A. Restoring function and esthetics in a patient with amelogenesis imperfecta: A clinical report. J. Prosthet. Dent. 90: 522-525, 2003.
• Pavlic A., Lukinma PL., Nieminen P. Severely hypoplastic amelogenesis imperfecta with taurodontizm. International Journal of Paediatric Dentistry 17: 259-266, 2007.
• Huen–TaiHo E. Amelogenesis imperfecta: A case report. Hong Kong Dental Journal 3: 123-127, 2006.