kidney

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References in periodicals archive ?
Autosomal-dominant medullary cystic kidney disease type 1: Clinical and molecular findings in six large Cypriot families.
Renal-cell carcinomas in end-stage kidneys: a clinicopathological study with emphasis on clear-cell papillary renal-cell carcinoma and acquired cystic kidney disease-associated carcinoma.
Contrast-enhanced CT and MRI are the imaging modalities of choice in characterizing cystic kidney masses.
While further research and testing is still needed, the work of doctors Sayer and Miles demonstrate that the abnormal cells in patients with cystic kidney disease do respond positively to drug treatments.
These were acute kidney injury, renal calculus disease, cystic kidney diseases, Malignancy, Glomerulonephritis, Ischemic nephropathy, chronic tubulointerstitial nephritis with distal RTA, Pyelonephritis.
44) According to Tickoo et al, (45) acquired cystic kidney disease (ACKD)-associated RCC is the most common cancer subtype developing in end-stage kidney.
By disabling the PKD1 gene in mice, researchers hope to produce rodents with the characteristic cystic kidney tubules.
0), renal disease (ICD-9-CM codes 582-586, 5900), obesity (ICD-9-CM code 278), and cystic kidney disease (ICD-9-CM codes 753.
Renal neoplasia and acquired cystic kidney disease in patients receiving long-term dialysis.
Constantinos Deltas, PhD, and Mr Gregory Papagregoriou, Department of Biological Sciences, University of Cyprus, Nicosia, Cyprus, in the next article focus on recent advances in the molecular biology and genetics of cystic kidney diseases and discuss the prospects and need for more widespread availability of laboratories for genetic testing.
Bunting, (29) in his review of cytogenesis, made the insightful comment that his 2 cases of cystic kidney disease differed morphologically and clinically from many previous reportedly cases.
This very task has become much faster and easier in most cases, although there are exceptions, such as the MCKD1 gene for medullary cystic kidney disease (MCKD) type 1, which remains stubbornly elusive (Figure 1 shows schematically the morbid cystic kidney chromosome map).
Earlier reports have depicted glomerular cysts and have portrayed similar cases of "congenital cystic kidney with glomerular cysts" (2,3,4) (Figure 1, A and B).
These kidneys can also develop acquired cystic kidney disease (ACKD), characterized by cystic dilatation of renal tubules, with an increasing incidence in parallel with the duration of dialysis (87% after 9 years).
Differential diagnosis of fetal hyperechogenic cystic kidneys unrelated to renal tract anomalies: A multicentre study.