A Unusal Presentation Of Bartter Syndrome

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dc.contributor.authorNitharsha, Prakash Men_US
dc.contributor.authorAnand, N Nagen_US
dc.date.accessioned2019-11-25T05:25:46Z
dc.date.available2019-11-25T05:25:46Z
dc.date.issued2019-08
dc.description.abstractBartter Syndrome is a rare congenital disease that manifests as hypokalemia, hyponatremia and hypotension. The disease occurs due to defective genes that are responsible for the reabsorption of certain electrolytes in the renal tubules. Hence it results in salt-wasting dyselectrolytemia. By its inheritable nature, the usual presentation of the disease is in the infants and children. But this case report presents an adult with symptoms of Bartter Syndrome which was discovered by chance while the patient was being treated for Acute gastroenteritis. Adult onset of Bartter Syndrome is incredibly rare and has been reported only in few other cases.en_US
dc.identifier.affiliationsJunior Resident, Department of General Medicine, Sree Balaji Medical College and Hospital, Chromepet, Chennai-44en_US
dc.identifier.affiliationsProfessor, Department of General Medicine, Sree Balaji Medical College and Hospital, Chromepet, Chennai-44 *Corresponding Authoren_US
dc.identifier.citationNitharsha Prakash M, Anand N Nag . Suprascapular Notch And Its Anatomical Variants. International Journal of Scientific Research. 2019 Aug; 8(8): 5-6en_US
dc.identifier.issn2277-8179
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/185254
dc.languageenen_US
dc.publisherWorld Wide Journalsen_US
dc.relation.issuenumber8en_US
dc.relation.volume8en_US
dc.subjecthypokalemiaen_US
dc.subjectBartter Syndromeen_US
dc.subjectkidneyen_US
dc.subjectdyselectrolytemiaen_US
dc.subjecthypomagnesemiaen_US
dc.titleA Unusal Presentation Of Bartter Syndromeen_US
dc.typeJournal Articleen_US
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