Try it
General Medicine · Nephrology and electrolytes: Bartter syndrome site of defect
Sample itemA 4-year-old child has failure to thrive, polyuria and muscle weakness. Investigations show potassium 2.6 mmol/L, metabolic alkalosis, raised renin and aldosterone, normal blood pressure and high urinary calcium excretion. There is no diuretic exposure. Which nephron segment is primarily affected?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
C. Thick ascending limb of the loop of Henle
Bartter syndrome results from defective salt reabsorption in the thick ascending limb, mimicking chronic loop diuretic use. The picture is hypokalaemic alkalosis with normal or low blood pressure, hyperreninaemic hyperaldosteronism and hypercalciuria. Gitelman syndrome, in the distal tubule, has low urinary calcium.
Option by option
A. Proximal convoluted tubule
Proximal tubule dysfunction causes bicarbonate, phosphate, glucose and amino acid wasting.
B. Cortical collecting duct principal cells
Collecting duct sodium channel overactivity causes hypertension with low renin and hypokalaemia.
C. Thick ascending limb of the loop of Henle (correct)
Correct. A loop-diuretic-like defect gives hypokalaemic alkalosis with hypercalciuria.
D. Distal convoluted tubule
Distal tubule defects mimic thiazides and cause hypocalciuria and hypomagnesaemia.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
More General Medicine questions
- EndocrinologyA 19-year-old with type 1 diabetes presents with vomiting, deep rapid breathing, fruity…
- ElectrolytesWhich is the earliest ECG change in hyperkalaemia?
- Infectious diseaseWhat is the drug of choice for Pneumocystis jirovecii pneumonia in a patient with advanc…
- NeurologyA chronic alcohol user is brought in confused, with nystagmus and an unsteady gait. What…