Ishwar Sidappa Hasabi1, Mahabaleshwar Mamadapur2, Chandrashekar Kachapur3, Sitaram N4, Kalinga B. E5
BACKGROUND
Bartter syndrome is a group of channelopathies with different genetic origins and molecular pathophysiologies, but sharing
common feature of decreased tubular transport of sodium chloride in thick ascending loop of Henle (TAL),1 although more
common in antenatal group. Classic adult variant of Bartter syndrome is a rare entity. We hereby present a rare adult variant
of classic Bartter syndrome.
