Abstract
Bartter syndrome is a rare salt-wasting nephropathy characterized by sporadic or inherited genetic defects in transporters and channels in the thick ascending limb of the loop of Henle and distal tubule of Nephron leads to renal potassium wasting with hypokalemia, metabolic alkalosis, increased renin-angiotensin-aldosterone system, normal blood pressure. Most of the cases have been noted in the pediatric age group and adult-onset cases are very rare. Here we report an unusual case report of Bartter's syndrome in a 52 years old male patient.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
