
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Chronic renal failure causes
Introduction
Overview
Overview
Common causes of chronic renal failure include diabetic nephropathy, hypertension, and glomerulonephritis. The commonest cause of stage 5 CKD in the U.S. is diabetes and is characterized by proteinuria and bilaterally enlarged kidneys. Hypertension is the second most common cause of Stage 5 CKD in the US, and often co-exists in diabetic patients.
Causes of Chronic Kidney Disease
Causes of Chronic Kidney Disease
- According to the National Kidney Foundation the 2 most important causes of CKD are diabetes and hypertension accounting for more than one third of all cases often indicating early detection strategies.[1]
- Beyond diabetes and hypertension other causes like glomerulonephritis, inherited disorders, chronic infections, and urinary tract obstruction account for most of the remaining cases.[2]
Common Causes
- Alport’s syndrome[3]
- Amyloidosis[4]
- Balkan endemic nephropathy
- Benign prostatic hyperplasia
- Chronic Glomerulonephritis
- Chronic Pyelonephritis
- Cystinosis[5]
- Diabetic nephropathy
- Glomerulosclerosis
- Goodpasture’s syndrome
- Hemolytic uremic syndrome
- Hereditary nephritides
- Hyperoxaluria
- Hypertensive nephrosclerosis
- IgA nephropathy
- Interstitial Nephritis
- Light chain disease
- Lupus nephritis
- Malignant hypertension
- Medullary cystic kidney disease
- Medullary sponge kidney
- Membranoproliferative Glomerulonephritis
- Membranous nephritis
- Metastatic prostate cancer
- Multiple Myeloma
- Nephrolithiasis
- Nephrosclerosis
- Nephrotic Syndrome
- Nephritic Syndrome
- Normocytic normochromic anemia
- Obstructive uropathy
- Oxalosis
- Papillorenal syndrome
- Polycystic kidney disease
- Proteinuria
- Prostate cancer
- Pyelonephritis
- Reflux nephropathy
- Renal artery stenosis
- Renal cell carcinoma
- Renal vein thrombosis
- Renal tubular acidosis
- Rheumatoid arthritis
- Scleroderma
- Sepsis
- Sickle cell disease
- Systemic sclerosis
- Thrombotic thrombocytopenic purpura
- Renal tubular acidosis
- Vasculitis
- Vesicoureteral reflux
- Wegener’s granulomatosis
Causes by Organ System
Causes in Alphabetical Order
- Ace inhibitors
- Acetominophen
- Action myoclonus
- Acute intermittent porphyriaÂ
- Acyclovir
- Adenine phosphoribosyltransferase deficiency
- Allopurinol
- Alport’s syndrome
- Alström syndrome
- Aminoglycosides
- Amphotericin b
- Amyloidosis
- Angiotensin-converting enzyme inhibitors
- Anticoagulants
- Aspirin
- Balkan endemic nephropathy
- Barakat syndrome
- Bardet-biedl syndrome
- Benign prostatic hyperplasia
- Bevacizumab
- Bismuth
- Carbon tetrachloride
- Carboplatin
- Carmustine
- Cefoxitin
- Chloroquine
- Chronic glomerulonephritis
- Chronic pyelonephritis
- Cimetidine
- Cisplatin
- Cocaine
- Congenital nephrotic syndrome
- Cyclosporine
- Cystinosis
- Dense deposit disease
- Dent disease
- Denys-drash syndrome
- Diabetes mellitus type 1
- Diabetes mellitus type 2
- Diabetic nephropathy
- Diflunisal
- Dioctophyma renale
- Erythromycin
- Essential hypertension
- Fabry’s disease
- Familial juvenile hyperuricemic nephropathy
- Febuxostat
- Ferumoxytol
- Fibronectin glomerulopathy
- Finnish congenital nephrotic syndrome
- Flucytosine
- Focal segmental glomerulosclerosis
- Foscarnet
- Frasier syndrome
- Furosemide
- Gadopentetate
- Galloway-mowat syndrome
- Gentamicin
- Glomerular hypertrophy
- Glomerulocystic kidney disease
- Glomerulonephritis
- Glomerulosclerosis
- Glycogenosis type 1b
- Goodpasture’s syndrome
- Gout
- Granulomatosis with polyangiitis
- Hemolytic uremic syndrome
- Hereditary nephritides
- Hereditary onycho-osteodysplasia
- Hydronephrosis
- Hydroxychloroquine
- Hyperkalemia
- Hyperlipidemia
- Hyperoxaluria
- Hyperoxaluria, primary type 1
- Hyperoxaluria, primary type 2
- Hyperoxaluria, primary type 3
- Hypertension
- Hypertensive nephrosclerosis
- Hyperuricemic nephropathy, familial juvenile type 1
- Hyperuricemic nephropathy, familial juvenile type 2
- Hypotension
- Hypovolemia
- Idiopathic membranous nephropathy
- Idiopathic multicentric osteolysis
- Ifosfamide
- Iga nephropathy
- Infliximab
- Interferons
- Interstitial nephritis
- Intraglomerular hypertension
- Isoniazid
- Jeune thoracic dystrophy syndrome
- Laxatives
- Lead
- Lecithin cholesterol acyltransferase deficiency
- Lesch-nyhan syndrome
- Light chain disease
- Lithium
- Loken senior syndrome
- Lomustine
- Lowe syndrome
- Lupus
- Lupus nephritis
- Mainzer-saldino disease
- Malignant hypertension
- Medullary cystic kidney disease
- Medullary cystic renal disease
- Medullary sponge kidney
- Membranoproliferative glomerulonephritis
- Membranous nephritis
- Mesalamine
- Metabolic acidosis
- Metastatic prostate cancer
- Methicillin
- Mitomycin c
- Multiple myeloma
- Nephritic syndrome
- Nephrolithiasis
- Nephrosclerosis
- Nephrotic syndrome
- Nitrosourea
- Normocytic normochromic anemia
- Nsaids
- Obstructive nephropathy
- Obstructive uropathy
- Oxalosis
- Pamidronate
- Papillorenal syndrome
- Penicillin
- Pentamidine
- Phenytoin
- Polycystic kidney disease
- Propylthiouracil
- Prostate cancer
- Protease inhibitors
- Proteinuria
- Pyelonephritis
- Quinine
- Radiocontrast agents
- Recurrent hereditary polyserositis
- Reflux nephropathy
- Renal artery stenosis
- Renal cell carcinoma
- Renal tubular acidosis
- Renal vein thrombosis
- Rheumatoid arthritis
- Rifampicin
- Saxagliptin
- Schistosoma haematobium
- Scleroderma
- Sensenbrenner syndrome
- Sepsis
- Sickle cell disease
- Sulfa-containing antibiotics
- Sulfonamides
- Sulindac
- Systemic hypertension
- Systemic sclerosis
- Tacrolimus
- Thiazides
- Thrombotic thrombocytopenic purpura
- Tizanidine
- Townes-brocks syndrome
- TrimethoprimÂ
- Tubulointerstitial disease
- Urinary tract obstruction
- Vancomycin
- Vasculitis
- Vesicoureteral reflux
- Wegener’s granulomatosis
- Xanthogranulomatous pyelonephritis
- X-linked hypophosphataemia
- X-linked recessive nephrolithiasis type 1
References
References
- ↑ Santamaria P, Boyce-Jacino MT, Lindstrom AL, Barbosa JJ, Faras AJ, Rich SS (February 1992). “HLA class II “typing”: direct sequencing of DRB, DQB, and DQA genes”. Hum. Immunol. 33 (2): 69–81. PMID 1563984.
- ↑ Levey AS, Coresh J, Balk E, Kausz AT, Levin A, Steffes MW; et al. (2003). “National Kidney Foundation practice guidelines for chronic kidney disease: evaluation, classification, and stratification”. Ann Intern Med. 139 (2): 137–47. PMID 12859163‎ Check
|pmid=value (help). - ↑ Schaeffer GW, St John JB, Sharpe FT (January 1972). “Effect of 6-benzylaminopurine on ATP levels and Me- 14 C incorporation into neutral and polar lipids during the release of dormant buds of Nicotiana tabacum”. Biochim. Biophys. Acta. 261 (1): 38–43. PMID 5012472.
- ↑ “[Comparison between the results obtained with androgen therapy and therapy with androgens and cytostatic drugs in advanced mammary carcinoma]”. Tumori (in Italian). 54 (4): 333–44. 1968. PMID 5697591.
- ↑ Croteau R, Kolattukudy PE (July 1974). “Biosynthesis of hydroxyfatty acid polymers. Enzymatic synthesis of cutin from monomer acids by cell-free preparations from the epidermis of Vicia faba leaves”. Biochemistry. 13 (15): 3193–202. PMID 4841061.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Â ; Associate Editor(s)-in-Chief: Aarti Narayan, M.B.B.S [2] Luke Rusowicz-Orazem, B.S.
