Bartter Syndrome
📋Overview
Bartter Syndrome is an inherited condition characterized by a defect in the thick ascending limb of the loop of Henle, which is the part of the kidney responsible for reabsorbing salt. This impairment typically leads to significant electrolyte imbalances, most notably low levels of potassium in the blood.
The condition can also result in metabolic alkalosis, a state where the blood becomes excessively alkaline because the kidneys cannot manage salt and fluid transport properly. These renal transport defects are the primary clinical features defining the disorder.
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Additional Resources
Medical codes (for reference)
UMLS CUI: C0004775Codes are provided for reference and interoperability. They are not a diagnosis.
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