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PCKDPolycystic Kidney Disease
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However, when CT and/or MRI remain inconclusive in a patient without clinical improvement, we recommend rapid referral to a polycystic kidney disease center.
New approaches to the autosomal recessive polycystic kidney disease patient with dual kidney-liver complications.
* Identify and understand important and diverse types of therapeutics under development for Polycystic Kidney Disease.
Autosomal recessive polycystic kidney disease (ARPKD) is a common inheritable cystic renal disease that has a profound effect on the growing fetus and on subsequent pregnancies, being fatal in 30% to 50% cases in the neonatal period.
Polycystic kidney disease. J Clin Hypertens (Greenwich).
Volume progression in polycystic kidney disease. N Engl J Med.
Failure to employ the known morphologic differences that exist between several of the major RCDs, such as dominant and recessive polycystic kidney disease and renal dysplasia, was prevalent in the early RCD classification literature.
Brother and sister Richard Routledge and Helen Lee both suffer from polycystic kidney disease, which claimed the lives of their father and great uncle.
He was diagnosed with polycystic kidney disease in 1999 and the organs steadily deteriorated.
Define autosomal dominant polycystic kidney disease.
Sadly, all three youngsters have also been diagnosed with polycystic kidney disease, the same devastating problem that Diane and her dad, John, now 67, suffer from.
Prevalence of the polycystic kidney disease and renal and urinary bladder ultrasonographic abnormalities in Persian and Exotic Shorthair cats in Italy.
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