kidney

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This novel and exciting platform presents multiple opportunities and a pipeline of potential therapeutics including treatments for glaucoma and cystic kidney disease.
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.
Such is the hypothesis of the origin of cystic kidney.
One of the earliest forays into the daunting arena of the classification of cystic kidney disease was by I.
The researchers reasoned that if they could interfere with the interaction of EGF and EGFR, and block the transmission of the signal from EGFR to the signaling cascade, they might prevent cell reproduction and cyst formation that is the hallmark and life-threatening complication of ARPKD, as well as ADPKD and other cystic kidney diseases.
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.
After adjusting for monthly income, geographic location, urbanization level, hypertension, diabetes, renal disease, obesity, cystic kidney disease, tobacco use disorder, and alcohol abuse, we found that, upon conditional logistic regression analysis (conditioned on sex, age, and index year), patients were more likely to have been previously diagnosed with UC before the index date when compared with controls (odds ratio [OR] 3.
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).
Medullary cystic kidney disease is an autosomal dominant condition with age-dependent penetrance than can lead to ESRD at any point from the third to the seventh decade of life.
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).
In hindsight, researchers probably should have suspected that cilia defects are behind cystic kidneys, says Maxence Nachury, a cell biologist and biochemist at Stanford.
Bladder agenesis patients may have associated malformations, such as genitals ambiguity, agenesis penis, cystic kidneys, solitary kidneys, anorrectal malformations, sacral anomalies, or multicystic dysplastic.