Classical Bartter syndrome in a 3 years old girl

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.