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Rare confluence: clinically diagnosed Bartter syndrome with sensorineural hearing loss in a young endosulfan-exposed
Samika Jhawar1, Rukmini Mysore Srikantiah2, Swayam Adappa1
1Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, India.
Abstract:
Bartter syndrome, a rare autosomal recessive disorder (1 in 1 000 000), causes salt wasting due to defects in the ion channels of the loop of Henle. In this case report, a young adolescent girl, who is a known case of Bartter syndrome and a recognised endosulfan exposure victim, presented with sensorineural hearing loss and multiple episodes of vomiting. She was treated with intravenous fluids, potassium supplementation and indomethacin. This case highlights the importance of early recognition and routine biochemical investigations to prevent complications of inherited tubulopathies.
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