Literature review of amelogenesis imperfecta with case report

Autor:	Sumathy C Chanmougananda, Kannan A Ashokan, Seethalakshmi C Ashokan, Anitha B Bojan, Ragu M Ganesh
Jazyk:	angličtina
Rok vydání:	2012
Předmět:	Amelogenesis imperfecta Mutation Enamel protease Inherited disease Dentistry RK1-715 Medical physics. Medical radiology. Nuclear medicine R895-920
Zdroj:	Journal of Indian Academy of Oral Medicine and Radiology, Vol 24, Iss 1, Pp 83-87 (2012)
Druh dokumentu:	article
ISSN:	0972-1363 0975-1572
DOI:	10.5005/jp-journals-10011-1266
Popis:	Amelogenesis impertecta (Al) is a diverse collection of inherited diseases that exhibit qualitative or quantitative tooth enamel defects in the absence of systemic manifestations. Also known by varied names, such as hereditary enamel dysplasia, hereditary brown opalescent teeth, this defect is entirely ectodermal, since mesodermal components of the teeth are basically normal. This article details a case of Al along with complete review which presents in his twin siblings with clinical, radiological and histopathological report.
Databáze:	Directory of Open Access Journals
Externí odkaz:	https://doaj.org/article/65421d639034477b9b2867bc4bb44376 Zobrazit plný text záznamu View record in DOAJ