Abstract
Bartter syndrome is rare genetic disorder of kidney characterized by hypokalemia, hypochloremia, metabolic alkalosis, hyponatremia, hypercalciuria, hyperreninemia, hyperaldosteronism with normal blood pressure. Here we report a case of 3 year old girl born of consanguious marriage, with complaints of not gaining weight with history of polyuria, polydipsia, having clinical and laboratory features of Bartter syndrome.
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