Bartter syndrome refers to a set of rare genetic disorders characterized by distinct kidney function abnormalities. These flaws impede the kidney's ability to reabsorb salt, resulting in electrolyte ...

Bartter syndrome and related renal tubulopathies comprise a group of rare, inherited disorders primarily affecting the reabsorption processes in the thick ascending limb of the loop of Henle and ...

This page lists all known medications that could potentially lead to 'Pseudo-Bartter syndrome' as a side effect. It's important to note that mild side effects are quite common with medications. The ...

Bartter syndrome type 3 is the result of several structural variants in the genome. By using long-read sequencing, Janine Altmüller and her team from the Max Delbrück Center, the BIH and University ...

Bartter syndrome type 3 is the result of several structural variants in the genome. By using long-read sequencing, Janine Altmüller and her team from the Max Delbrück Center, the BIH and University ...

The course of the disease is individual and symptoms can range from mild to severe and life-threatening. Clinical findings include polyuria, hypovolemia, salt craving, growth retardation, vomiting, ...

Apical (luminal) uptake of sodium chloride in the thick ascending limb cells is mediated by the sodium–potassium–chloride cotransporter (NKCC2). Potassium recirculates into the lumen by way of apical ...

Since the description in 1962 of a syndrome of "hyperplasia of the juxtaglomerular complex with hyperaldosteronism and hypokalemic alkalosis" 1 a number of reports of the same and of similar syndromes ...