CAKUT


Also found in: Acronyms.

CAKUT

congenital anomalies of the kidneys and urinary tract.
References in periodicals archive ?
It is concluded that Congenital anomalies of kidney and urinary tract (CAKUT) was found to be the underlying etiology of chronic kidney disease in majority of our children who underwent CAPD.
The Outcome of Continuous Ambulatory Peritoneal Dialysis in Children: A Single Center Experience
Data of 30 patients with CAKUT aged between 1 and 41 months and 32 healthy children were included in the study.
Bayley- III Scores of Children with Congenital Anomalies of the Kidney and Urinary Tract
We found structural abnormalities of urinary tract in 14% and almost all had CAKUT except one who had stone disease.
Functional and structural abnormalities of the kidney and urinary tract in severely malnourished children - A hospital based study
Etiology of chronic kidney disease in children CKD ESRD Etiology Percentage (Range) Etiology Percentage (Range) CAKUT 48-59% CAKUT 34-43% GN 5-14% GN 15-29% HN 10-19% HN 12-22% HUS 2-6% HUS 2-6% Cystic 5-9% Cystic 6-12% Ischemic 2-4% Ischemic 2% Rare causes include congenital NS, metabolic diseases, cystinosis/Miscellaneous causes depend on how such entities are classified.
Averting the Legacy of Kidney Disease-Focus on Childhood
Our research group has recently reported a correlation between high urinary levels of CXCL8/IL-8 and reduced glomerular filtration rate in CAKUT patients, suggesting that this chemokine might be associated with renal scarring and CKD [12].
Chemokines as potential markers in pediatric renal diseases
* Early diagnosis and appropriate management can prevent development of complications in many infants with CAKUT.
Common paediatric renal conditions: few children in South Africa have access to dialysis or renal transplantation, so it is important to recognise kidney disease early enough to prevent progression to end-stage disease
In this section, we reported studies that associated cytokines with relevant clinical consequences of CAKUT such as acute pyelonephritis, urinary tract obstruction, and renal scarring.
Interactions between cytokines, congenital anomalies of kidney and urinary tract and chronic kidney disease
Knowledge of the embryologic development of the kidney would appear to provide a logical basis for explaining departures from normal renal development and was especially popular for many CAKUT lesions.
The classification of renal cystic diseases and other congenital malformations of the kidney and urinary tract
ADPKD was the most common inherited kidney disease diagnosis, accounting for 40.3% of cases, followed by CAKUT (11.5%), Alport syndrome (9.4%), and ARPKD (7.2%) (Table 5).
End-Stage Kidney Failure in Oman: An Analysis of Registry Data with an Emphasis on Congenital and Inherited Renal Diseases
* congenital abnormalities of the kidney and urogenital tract (CAKUT), e.g.
Paediatric chronic kidney disease
Prophylactic antibiotic treatment prevents the recurrence of urinary tract infections in children with CAKUT
February 2012 - anatomical pathology
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