polycystic kidney disease

(redirected from Cystic kidney disease)
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Synonyms for polycystic kidney disease

kidney disease characterized by enlarged kidneys containing many cysts

References in periodicals archive ?
[ClickPress, Tue Apr 16 2019] The development of various techniques, increasing number of patients going for dialysis, and favorable reimbursement policies and government initiatives propel the growth of the Acquired Cystic Kidney Disease Treatment Market .
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing.
Barrio-Lucia, "A novel pattern of mutation in uromodulin disorders: autosomal dominant medullary cystic kidney disease type 2, familial juvenile hyperuricemic nephropathy, and autosomal dominant glomerulocystic kidney disease," American Journal of Kidney Diseases, vol.
Medullary cystic kidney disease (MCKD) is a progressive tubulointerstitial nephropathy leading to end-stage renal disease (ESRD) and need for dialysis or kidney transplantation.[1] MCKD occurs in adulthood with a variable age of onset, ranging from 20 to 70 years within and between families.[2],[3] The manifestations of MCKD are highly variable and nonspecific.
On imaging, ACD-RCC appears as a heterogeneously enhancing solid mass either within the atrophic kidneys or kidneys with multiple cysts secondary to acquired cystic kidney disease (Figure 8).
Children affected by the illness have a range of problems, including learning difficulties, movement problems, loss of eyesight and life-threatening cystic kidney disease, often leading to total kidney failure by the age of 13.
The incidence of RCC in native kidney of renal transplant recipient patients varies between 0.3% and 4.8%.7 Male gender, African-American race, recipients aged at least 65 years, a donor aged at least 50 years, microscopic haematuria, patients having a long pre-transplant dialysis interval and acquired cystic kidney disease (ACKD) are significantly associated with the risk of native kidney malignancy in renal transplant recipients.7 However, another study found no significant relationship between RCC occurrence and patient age, dialysis (when initiated, type and duration), transplantation, drug regimen or incidence of ACKD.
Diabetes 44% High blood pressure 28% Other causes 19% Glomerular disease 7% Cystic kidney disease 2% SOURCE: NATIONAL KIDNEY AND UROLOGIC DISEASES INFORMATION CLEARINGHOUSE Note: Table made from pie chart.
When the cases of ESRD were categorized by nine possible causes--diabetes, hypertension, glomerulonephritis, hereditary nephritis, interstitial nephritis, cystic kidney disease, secondary glomerulonephritis, drug-induced, and other causes--the clear majority of cases among subjects who had hematuria in adolescence were found to be due to glomerular disease.
But genetic testing has the limitations of only detecting the autosomal dominant form of PKD and not other forms of cystic kidney disease. Additionally, genetic testing is unable to assess the severity of the disease.
Even in his personal life, Stein was involved in his community, raising money for cancer research and AIDS causes locally in Danbury, as well as those afflicted with cystic kidney disease, said Browning.
In 2003, 23,000 people with cystic kidney disease (mostly PKD) received dialysis or a kidney transplant, making it the fourth leading cause of kidney failure in the country.
4 of infantile cystic kidney disease. He was 1 day old.
* Acquired cystic kidney disease (ACKD) develops in association with long-term kidney problems, especially in patients who have kidney failure and who have been on dialysis for a long time.