Amelogenesis Imperfecta - A Case Report.

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dc.contributor.authorReddy, Y Narendranath
dc.contributor.authorReddy, E Shiva Prasad
dc.date.accessioned2016-02-22T07:03:09Z
dc.date.available2016-02-22T07:03:09Z
dc.date.issued2010-01
dc.description.abstractAmelogenesis imperfecta (Al) is a diverse collection of inherited diseased that exhibit quantitative or qualitative tooth enamel defects in the absence of systemic manifestations. Also known by varied names such as Hereditary of enamel dysplasia, Hereditary brown enamel, Hereditary brown opalescent teeth, this defect is entirely ectodermal, since mesodermal components of the teeth are basically normal. The Al trait can be transmitted by either autosomal dominant, autosomal recessive, or X-linked modes of inheritance. It is necessary to diagnose the case and provide durable functional and esthetic management of these patients, where the unaesthetic appearance has a definite negative psychological impact.en_US
dc.identifier.citationReddy Y Narendranath, Reddy E Shiva Prasad. Amelogenesis Imperfecta - A Case Report . Annals and Essences of Dentistry. 2010 Jan-Mar; 2(1): 19-21.en_US
dc.identifier.issn0975-8798
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/173769
dc.language.isoenen_US
dc.source.urihttps://www.aedj.in/2.1.19-21en_US
dc.subjectAmelogenesis imperfectaen_US
dc.subjectenamelen_US
dc.subjectdentalen_US
dc.subjectgeneticen_US
dc.titleAmelogenesis Imperfecta - A Case Report.en_US
dc.typeArticleen_US
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