Amelogenesis imperfecta with renal disease - a report of two cases
Amelogenesis imperfecta with renal disease - a report of two cases
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DOI：
10.1111/j.1600-0714.2007.00615.x
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发表时间：
2007-11-01
影响因子：
3.3
通讯作者：
Ranganathan, K.
中科院分区：
文献类型：
--
作者：
Elizabeth, J.;Priya, E. Lakshmi;Ranganathan, K.
釉质发育不全症（AI）是一系列以釉质形成异常为特征的发育状况的统称。阿尔茨海默病通常与全身性发现无关；然而，文献中报道了一些与综合征和代谢紊乱相关的Al病例。我们报告了两例以肾脏疾病为表现的人工智能病例，从而强调了在早期阶段认识到这种可能关联的重要性，因为在某些情况下，人工智能可能是肾脏疾病的标志。
Amelogenesis imperfecta (AI) is a collective term for a number of developmental conditions characterized by abnormal enamel formation. Al is usually not associated with generalized findings; however, a few cases of Al associated with syndromes and metabolic disorders have been reported in the literature. We report two cases of Al presenting with renal disease and thereby highlight the importance of recognizing this possible association at an early stage, as Al in some cases, may be a marker of renal disease.