Autosomal Dominant Polycystic Kidney Disease: Presentation, Complications, and Prognosis
Referencess (33)
- et al.
A clinical review of polycystic disease in 53 patients
J Urol
(1967) - et al.
Adult polycystic kidney disease: A review of 100 cases
J Urol
(1977) - et al.
Management of infected polycystic kidneys
J Urol
(1979) - et al.
Rate of functional deterioration in polycystic kidney disease
Kidney Int
(1983) Nephrotic syndrome in polycystic renal disease
J Urol
(1971)- et al.
Cyst fluid antibiotic concentrations in polycystic kidney disease: Differences between proximal and distal cysts
Kidney Int
(1981) The eleventh report of the human renal transplant registry
JAMA
(1975)- et al.
Combined report on regular dialysis and transplantation in Europe VIII, 1976
Proc Eur Dial Transplant Assoc
(1977) - et al.
Adult polycystic disease of the kidneys (Potter type III)
JAMA
(1972) Bilateral polycystic disease of the kidneyszzz A follow up of two hundred and eighty-four patients and their families
Acta Med Scand
(1975)
Bilateral polycystic kidney disease: Review of 94 cases
Arch Surg
Congenital polycystic disease of the kidney: Review of the literature and data in 207 cases
Am J Med Sci
Congenital polycystic diseasezzz A clinical and therapeutic study of 366 cases
JAMA
The surgical management of polycystic renal disease
Surg Gynecol Obstet
Renal function studies in polycystic disease of the kidneys—With observations on the effects of surgical decompression
N Engl J Med
Some different types of essential hypertension: Their cause and prognosis
Am J Med Sci
Cited by (90)
African American polycystic kidney patients receive higher risk kidneys, but do not face increased risk for graft failure or post-transplant mortality
2021, American Journal of SurgeryCitation Excerpt :On the other hand, some afflicted individuals reach end-stage renal failure (ESRF) in the fourth decade. Ultimately about 60% of ADPKD reach ESRF by their sixth decade.4,15,16 Despite the genetic nature of this disease, the heterogeneity displayed in the ADPKD population suggests that other components influence the progression of the disease.
KHA-CARI Autosomal Dominant Polycystic Kidney Disease Guideline: Management of Renal Stone Disease
2015, Seminars in NephrologyCitation Excerpt :Accordingly, heightened awareness and potential modification of the standard clinical approach is required compared to patients presenting with nephrolithiasis who do not have ADPKD.2,3 The prevalence of nephrolithiasis in ADPKD may be 5 to 10 times higher compared to the general population.4 This increased risk is probably due to reduced urinary flow (and stasis) in renal tubules and calyces due to compression from expanding renal cysts as well as underlying urinary metabolic abnormalities.5
Management of Stones in Abnormal Situations
2013, Urologic Clinics of North AmericaCitation Excerpt :There are 2 variants: the polycystin-1 (PKD-1) mutation is associated with onset of cysts at an earlier age and end-stage renal failure by the fifth or sixth decade of life. Nephrolithiasis in ADPKD is 5 to 10 times more common than in the general population.69 There are both anatomic and metabolic reasons for this.
Renal failure and cystic kidney diseases
2011, Journal de Radiologie