polycystic kidney disease

(redirected from Autosomal dominant polycystic kidney disease)
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  • noun

Synonyms for polycystic kidney disease

kidney disease characterized by enlarged kidneys containing many cysts

References in periodicals archive ?
Extrarenal manifestations of autosomal dominant polycystic kidney disease.
Potts, MD, Thoracic aortic dissection in a patient with autosomal dominant polycystic kidney disease.
Ambulatory blood pressure correlates with renal volume and number of renal cysts in children with autosomal dominant polycystic kidney disease.
Discuss how the FNP PCP should best treat and monitor a patient with autosomal dominant polycystic kidney disease.
Kaehny WD, Everson GT: Extrarenal manifestations of autosomal dominant polycystic kidney disease.
In line with our strategy, the autosomal dominant polycystic kidney disease diagnostic patent provides us with another excellent licensing and partnering opportunity.
Autosomal dominant polycystic kidney disease (adult polycystic kidney disease, Potter type III disease) is the fourth-most common cause of end-stage renal disease.
Autosomal dominant polycystic kidney disease with anticipation and Caroli's disease associated with a PKD1 mutation.
1-12) Although most patients with some of the more common forms of maldevelopment, such as bifid ureter and horseshoe kidney, may have few significant complications, collectively, RCD/CAKUT represent the most common cause of end-stage renal disease in children, accounting for 40% to 50% of cases, and includes autosomal dominant polycystic kidney disease, the most common type of RCD and the fourth leading cause of end-stage renal disease in adults.
Three patients died; 1 after 16 months from a cerebral bleed probably related to autosomal dominant polycystic kidney disease (ADPKD), 1 from catheter-related sepsis after 14 months, and 1 from further catheter occlusion after 9 months.
This growth is primarily attributed to the expected launch of Samsca (tolvaptan) for the treatment of patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD).
Current knowledge on cyst initiation and development mainly comes from investigations on autosomal dominant polycystic kidney disease (ADPKD), in which cystic pathology is believed to be the result of abnormal cell proliferation and deregulated apoptosis, increased secretion of fluids into the tubular lumen, irregular cell-matrix interactions, and defective cellular polarity.
Nasdaq:AVII)(Nasdaq:AVIIW)(Nasdaq:AVIIZ), today announced the final results from its NEUGENE(R) antisense drug (AVI-4126) study in adult patients with autosomal dominant polycystic kidney disease (PKD).
13,16,21-25) With better understanding of the underlying genetic mutations in heritable GCK, a more specific use of terms is gaining popularity and the older classification of GCKD as a variant only--of autosomal dominant polycystic kidney disease (ADPKD)--no longer appears justified.
Nasdaq:AVII)(Nasdaq:AVIIW)(Nasdaq:AVIIZ) today announced that its NEUGENE(R) antisense drug (AVI-4126) proved safe in adult patients with autosomal dominant Polycystic Kidney Disease (PKD).
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