Inborn errors of renal tubular transport

Inborn errors of renal tubular transport
Inborn errors of renal tubular transport
	a-d)Gitelman syndrome viewed via light microscope and electron microscopy

Inborn errors of renal tubular transport are metabolic disorders which lead to impairment in the ability of solutes, such as salts or amino acids, to be transported across the brush border of the renal tubule. This results in disruptions of renal reabsorption.Examples of these disorders include Iminoglycinuria, renal tubular acidosis and Gitelman syndrome.^[1]^{[additional citation(s) needed]}

References

↑ "Renal Tubular Acidosis | NIDDK". National Institute of Diabetes and Digestive and Kidney Diseases. Archived from the original on 9 January 2021. Retrieved 21 December 2022.

This article about an endocrine, nutritional, or metabolic disease is a stub. You can help MDWiki by expanding it.

v t e Kidney disease
Glomerular disease	See Template:Glomerular disease
Tubules	Renal tubular acidosis proximal distal Acute tubular necrosis Genetic Fanconi syndrome Bartter syndrome Gitelman syndrome Liddle's syndrome
Interstitium	Interstitial nephritis Pyelonephritis Balkan endemic nephropathy
Vascular	Renal artery stenosis Renal ischemia Hypertensive nephropathy Renovascular hypertension Renal cortical necrosis
General syndromes	Nephritis Nephrosis Renal failure Acute renal failure Chronic kidney disease Uremia
Other	Analgesic nephropathy Renal osteodystrophy Nephroptosis Abderhalden–Kaufmann–Lignac syndrome Diabetes insipidus Nephrogenic Renal papilla Renal papillary necrosis Major calyx/pelvis Hydronephrosis Pyonephrosis Reflux nephropathy