نتایج جستجو برای: cakut

تعداد نتایج: 175  

Journal: :Anales de pediatria 2015
M L Palacios Loro D K Segura Ramírez F A Ordoñez Álvarez F Santos Rodríguez

The congenital abnormalities of kidney and urinary tract (CAKUT) are disorders with a high prevalence in the general population, with urinary tract dilations being the most frequent. CAKUT also account for the most important cause of chronic kidney disease in childhood. This paper focuses on the role of the primary care paediatrician in the diagnosis, assessment, and follow-up of children with ...

Journal: :Prilozi 2017
Aleksandra Janchevska Zoran Gucev L Tasevska-Rmus Velibor Tasic

INTRODUCTION Congenital anomalies of the kidney and urinary tract (CAKUT) represent several types of malformations with occurrence of 1 in about 500 live births. OBJECTIVE Small for gestation age (SGA) may influence in prevalence of CAKUT and progression of chronic kidney disease (CKD) in children. The aim of this study was to elaborate our experiences with detected CAKUT in a cohort of SGA b...

Journal: :Jornal de pediatria 2014
Geisilaine Soares dos Reis Ana Cristina Simões E Silva Izabella Silva Freitas Thiago Ramos Heilbuth Luiz Armando de Marco Eduardo Araújo Oliveira Débora Marques Miranda

OBJECTIVE To determine the frequency of different phenotypes for congenital anomalies of the kidney and urinary tract (CAKUT) in a Brazilian sample, and to evaluate the association between the CAKUT phenotypes and the BMP4 gene. METHODS In this study, 457 Brazilian individuals were analyzed in an attempt to establish the association between the BMP4 gene and the CAKUT diagnosis. A case-contro...

Journal: :Prilozi 2017
Nadica Ristoska-Bojkovska

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...

2018
Herui Wang Chi Zhang Xiaowen Wang Yaru Lian Bin Guo Miao Han Xiaoe Zhang Xiaoting Zhu Sixian Xu Zengli Guo Yunli Bi Qian Shen Xiang Wang Jiaojiao Liu Yuan Zhuang Ting Ni Hong Xu Xiaohui Wu

Congenital anomalies of the kidney and urinary tract (CAKUT) are among the most common developmental defects in humans. Despite of several known CAKUT-related loci (HNF1B, PAX2, EYA1, etc.), the genetic etiology of CAKUT remains to be elucidated for most patients. In this study, we report that disruption of the Holliday Junction resolvase gene Gen1 leads to renal agenesis, duplex kidney, hydron...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010
Shazia Ashraf Bethan E Hoskins Hassan Chaib Julia Hoefele Andreas Pasch Pawaree Saisawat Friedrich Trefz Hans W Hacker Gudrun Nuernberg Peter Nuernberg Edgar A Otto Friedhelm Hildebrandt

BACKGROUND Congenital anomalies of the kidney and urinary tract (CAKUT) account for the majority of end-stage renal disease in children (50%). Previous studies have mapped autosomal dominant loci for CAKUT. We here report a genome-wide search for linkage in a large pedigree of Somalian descent containing eight affected individuals with a non-syndromic form of CAKUT. METHODS Clinical data and ...

2018
Amelie T van der Ven Birgit Kobbe Stefan Kohl Shirlee Shril Hans-Martin Pogoda Thomas Imhof Hadas Ityel Asaf Vivante Jing Chen Daw-Yang Hwang Dervla M Connaughton Nina Mann Eugen Widmeier Mary Taglienti Johanna Magdalena Schmidt Makiko Nakayama Prabha Senguttuvan Selvin Kumar Velibor Tasic Elijah O Kehinde Shrikant M Mane Richard P Lifton Neveen Soliman Weining Lu Stuart B Bauer Matthias Hammerschmidt Raimund Wagener Friedhelm Hildebrandt

Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common cause (40-50%) of chronic kidney disease (CKD) in children. About 40 monogenic causes of CAKUT have so far been discovered. To date less than 20% of CAKUT cases can be explained by mutations in these 40 genes. To identify additional monogenic causes of CAKUT, we performed whole exome sequencing (WES) and homozygosi...

Journal: :Kidney International 2021

Although a rare disease, bilateral congenital anomalies of the kidney and urinary tract (CAKUT) are leading cause end stage disease in children. Ultrasound-based prenatal prediction postnatal survival CAKUT pregnancies is far from accurate. To improve prediction, we conducted prospective multicenter peptidome analysis amniotic fluid spanning 140 evaluable fetuses with CAKUT. We identified signa...

2011
Renfang Song Samir S. El-Dahr Ihor V. Yosypiv

The kidney plays a fundamental role in the regulation of arterial blood pressure and fluid/electrolyte homeostasis. As congenital anomalies of the kidney and urinary tract (CAKUT) constitute one of the most common human birth defects, improved understanding of the cellular and molecular mechanisms that lead to CAKUT is critical. Accumulating evidence indicates that aberrant signaling via recept...

2014
Mahmood Dhahir Al-Mendalawi

OBJECTIVE To study the prevalence, pattern of distribution, and the outcome of different types of kidney and urinary tract anomalies (CAKUT) diagnosed during the antenatal period. The second objective is to test the accuracy of antenatal diagnosis of CAKUT. MATERIALS AND METHODS In a cross-sectional hospital-based study, all cases diagnosed antenatally with urinary tract anomalies at King Abd...

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