POS-445 ACUTE PYELONEPHRITIS IN CHILDREN WITH CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT (CAKUT): ABOUT A SERIES OF 45 CASES
نویسندگان
چکیده
منابع مشابه
Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).
Congenital anomalies of the kidneys and urinary tract (CAKUT) are found in 3-6 out of 1.000 of the newborns, or according to some statistics they are represented in 0.5% of all pregnancies. Congenital abnormalities of the kidneys and urinary tract present a family of diseases of various anatomic spectrum, including renal anomalies, and anomalies of the bladder and urethra. The study was retrosp...
متن کاملCongenital Anomalies of the Kidney and the Urinary Tract (CAKUT)
This article reviews the majority of Congenital Anomalies of the Kidney and Urinary Tract (CAKUT) with emphasis in Pediatric Pathology describing and illustrating lesions as varied as ureteral duplications, ureteropelvic junction obstruction, horseshoe kidney, posterior urethral valve and prune belly syndrome, obstructive renal dysplasia, nonmotile ciliopathies and several syndromes associated ...
متن کاملA holistic approach to CAKUT (Congenital Anomalies of the Kidney and Urinary Tract)
Keywords CAKUT (Congenital Anomalies of the Kidney and Urinary Tract), urinary tract infection, chronic kidney disease, follow-up. Editorial " Structure does not determine Function or vice versa, but both are simply different ways of regarding and describing the same thing. "
متن کاملPTHrP-related Hypercalcaemia in Infancy and Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)
BACKGROUND Severe hypercalcaemia is a rare but clinically significant condition in infancy and childhood. Parathyroid hormone-related peptide (PTHrP)-mediated hypercalcaemia resulting from a malignancy is rare and only a handful of case reports have outlined its incidence alongside a benign condition. OBJECTIVES To describe the diagnostic workup and management of an infant with hypercalcaemia...
متن کاملCHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT).
BACKGROUND Recently, we identified a microduplication in chromosomal band 1q21.1 encompassing the CHD1L/ALC1 gene encoding a chromatin-remodelling enzyme in congenital anomalies of the kidneys and urinary tract (CAKUT) patient. METHODS To explore the role of CHD1L in CAKUT, we screened 85 CAKUT patients for mutations in the CHD1L gene and performed functional analyses of the three heterozygou...
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ژورنال
عنوان ژورنال: Kidney International Reports
سال: 2021
ISSN: 2468-0249
DOI: 10.1016/j.ekir.2021.03.470