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10.4103/ijn.IJN_203_16

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suck abstract from ncbi


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pmid28904439
      Indian+J+Nephrol 2017 ; 27 (5 ): 399-401
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  • Association of Amelogenesis Imperfecta and Bartter s Syndrome #MMPMID28904439
  • Kumar ACV ; Alekya V ; Krishna MSVV ; Alekya K ; Aruna M ; Reddy MHK ; Sangeetha B ; Ram R ; Kumar VS
  • Indian J Nephrol 2017[Sep]; 27 (5 ): 399-401 PMID28904439 show ga
  • 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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