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Samples in periodicals archive:
In children, the most common causes for CLKT are congenital diseases affecting both liver and kidney, such as primary hyperoxaluria type 1 (PH1) and autosomal recessive polycystic kidney disease (ARPKD).
Lola and Nicole were both born with the rare Autosomal Recessive Polycystic Kidney Disease, which causes cysts to appear in the tubes that produce and transport urine and bile.
Her 10-year-old sister Nicole, also had Autosomal Recessive Polycystic Kidney Disease, but can now eat what she likes after a double organ transplant.
When Sebastian died in 2009, from the rare kidney condition Autosomal Recessive Polycystic Kidney Disease, she and Mr Hall made memory boxes for Louis and Dominic, putting in photos and toys of their brother to make sure they keep his memory alive.
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.
Researchers at the Mayo Clinic have identified and fully characterized the gene that causes autosomal recessive polycystic kidney disease (ARPKD), raising hopes of a treatment and eventual cure for infants born with ARPKD.
The chief indication for CPLKT is for rare congenital diseases affecting both liver and kidney (such as primary hyperoxaluria type 1 and autosomal recessive polycystic kidney disease with hepatic fibrosis).
The data suggest the exciting possibility that targeting the activity of PKD1 may be beneficial for treatment of isolated polycystic liver disease, childhood recessive polycystic kidney disease and even a subset of adult ADPKD," Somlo said.