Association of Amelogenesis Imperfecta and Bartter's Syndrome

Bartter's syndrome is an autosomal recessive renal tubular disorder characterized by hypokalemia, hypochloremia, metabolic alkalosis, and hyperreninemia with normal blood pressure. Bartter's syndrome is associated with hypercalciuria and nephrocalcinosis. Amelogenesis imperfecta (AI) is a...

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Detalles Bibliográficos
Autores principales: Kumar, A. C. V., Alekya, V., Krishna, M. S. V. V., Alekya, K., Aruna, M., Reddy, M. H. K., Sangeetha, B., Ram, R., Kumar, V. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590420/
https://www.ncbi.nlm.nih.gov/pubmed/28904439
http://dx.doi.org/10.4103/ijn.IJN_203_16
Descripción
Sumario:Bartter's syndrome is an autosomal recessive renal tubular disorder characterized by hypokalemia, hypochloremia, metabolic alkalosis, and hyperreninemia with normal blood pressure. Bartter's syndrome is associated with hypercalciuria and nephrocalcinosis. Amelogenesis imperfecta (AI) is a group of hereditary disorders that affect dental enamel. AI could be part of several syndromes. The enamel renal syndrome is the association of AI and nephrocalcinosis. We report two patients of AI with Bartter's syndrome.

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