Problems on prenatal diagnosis of kidneys duplication in the embryogenesis view

Author(s):  
V.N. Osadshaya, O.A. Grammatikova, E.D. Lutaya et all

In this article we consider the most crucial stages of the embryology of the urinary system, which help to explain the mechanisms of duplication of the kidneys (complete/incomplete) and other forms of the urinary system development abnormalities. We report on our experience with the prenatal diagnosis of duplication of the kidneys in two fetuses. These cases represent dynamics and variability of the pathological process.

2022 ◽  
pp. 41-45
Author(s):  
A. Nее ◽  
E. V. Sergeeva ◽  
O. G. Bykova ◽  
O. V. Semeshina

Objective: To study main clinical and laboratory peculiarities of the course of urinary tract disease among children aged from newborns to 3 years old.Methods: Research design is a prospective controlled clinical research. 102 (60.71±3.77 %) children having urinary tract infection without accompanying abnormalities of the urinary system development were included in the first group. 66 (39.29±3.77 %) children having infection of the urinary tract amid congenital kidney defect.Results: Comparative evaluation of the results of complex examination of both groups showed that urinary tract infection is characterized by intoxication, pain and dysuric syndroms. The presence of accompanying kidneys and urinary tract abnormality development defined the latent course of the disease in every second child (59.09%) and supports the early development of renal infection (during first six months after birth).Conclusions: It’s necessary to conduct the search of diagnostics markers and predictors of the infection of the urinary tract among children of the first years of life, especially if there is an abnormality of the organs of urinary system.


2021 ◽  
Vol 74 (3) ◽  
pp. 450-454
Author(s):  
Oleksandr Ye. Dobrovanov

The aim: To compare the effectiveness and sensitivity of prenatal and postnatal diagnostics in the diagnosis of congenital malformations of the urinary system in the Slovak Republic. Materials and methods: Data of postnatal sonographic screening of congenital developmental malformations of the urinary system in Slovak Republic including 2017 were identified and updated using a questionnaire survey, 38,496 newborns were involved. Statistical data on the proportion of prenatal diagnosis for the years 1995, 2000, 2005, 2008 and 2013-2016 were provided from the National Register of Congenital Defects. The chi2-test and t-test were applied to assess the sensitivity differences. Results: The study showed a low sensitivity of prenatal diagnosis with its maximum in 2016, reaching 32.3% and a minimum in 2005-2008 (8.0 – 8.4%). The sensitivity of postnatal diagnostics for selected years has always been a stable indicator and reaches 99.6%. Conclusions: Available statistical data confirm that prenatal diagnostics of congenital developmental malformations of the urinary system in the Slovak Republic is not perfect. Our work underlines the importance, or we should rather say inevitability of postnatal ultrasound screening for congenital developmental anomalies in the kidneys.


2012 ◽  
Vol 8 (5) ◽  
pp. 535-543 ◽  
Author(s):  
İbrahim Karnak ◽  
Pergin Atilla ◽  
Sevda Müftüoğlu

2020 ◽  
Vol 10 (3) ◽  
pp. 220-226
Author(s):  
Miraç Özalp ◽  
Hatice Sonay Yalçın Cömert ◽  
Ömer Demir ◽  
Hidayet Şal ◽  
Turhan Aran ◽  
...  

Author(s):  
Svetlana P. Kokoreva ◽  
Natalya V. Kazartseva

A significant increase in the incidence of enterovirus infections (EVI) with the development of multiple organ damage does not exclude the involvement of the urinary system organs in the pathological process. Materials and methods. 151 EVI children (103 cases with enterovirus meningitis (EVM), 48 children with other forms of EVI without damage of central nervous system) aged from 1 to 18 years. The frequency and nature of changes in urinary sediment and kidney function in patients with various EVI forms were studied. A highly sensitive marker of acute kidney injury - KIM-1 was used as a marker along with standard methods (determination of blood creatinine level with calculation of glomerular filtration rate) in 25 EVM patients. Results. Pathological changes in urinary sediment in EVI are registered in 37.75% of cases (27.1-42.72%, depending on the clinical form), more often in preschool children, are represented by unexpressed proteinuria and abacterial leukocyturia, and are of a short-term transient nature. 40% of EVM children patients showed an increase in the KIM-1 level above the standard values. Conclusion. The detection of KIM-1 in the urine of EVM children patients indicates the possible development of acute transient tubulointerstitial renal damage. At risk there are children with cerebrospinal fluid pleocytosis greater than 200×106/L, abacterial leukocyturia, and decreased glomerular filtration rate.


2018 ◽  
Vol 26 (1) ◽  
pp. 1-6
Author(s):  
Ezgi Hürcan ◽  
Alper Biler ◽  
Atalay Ekin ◽  
Gökhan Tosun ◽  
Cüneyt Eftal Taner

Author(s):  
O. Dobrovanov ◽  
K. Kralinsky ◽  
J. Molcan ◽  
V. P. Kovalchuk

The results of diagnostics of obstructive uropathies and some other congenital changes in the kidneys, which were obtained using neonatal sonographic screening for 2018 in the neonatal unit of the Third Children’s Clinic of the Slovak Medical University, are presented. The results of thisstudy were compared with statistical data from the National Centerfor Medical Information of Slovakia for 2017–2018. The disadvantages of prenatal diagnosis in different regions of the Slovak Republic, as well as some administrative disadvantages of neonatal ultrasound screening at the present time, are shown. The importance of early diagnosis of obstructive uropathy is also shown.


Author(s):  
G. Grebinichenko ◽  
I. Gordienko ◽  
O. Sliepov ◽  
O. Tarapurova ◽  
V. Soroka ◽  
...  

Purpose - to present a method of prenatal assessment of viscero-abdominal disproportion in fetuses with gastroschisis during two-dimensional ultrasound examination, to compare prenatally determined indices with postnatal clinical data. Materials and methods. Extended measurements of the abdominal cavity and eventrated organs in 161 fetuses with gastroschisis were performed at different terms of pregnancy. Postnatal intraoperative data and general clinical outcomes were compared in 74 cases depending on the results of prenatal measurements: the presence and degree of pathological changes in the eventrated intestine, the degree of viscero-abdominal disproportion and type of surgical correction, presence of associated intestinal malformations and mortality. Results. A methodology for determining the index of viscero-abdominal disproportion in fetuses with gastroschisis and a working classification of its degrees was proposed. The disproportion was absent in the 2nd trimester in 80.5% of fetuses, and in the 3rd trimester only in 40.7%. During the 2nd trimester, the degree of VAD changed in 1.8% of cases, during the 3rd trimester in 11.1% of cases. Among the 55 fetuses examined in both the 2nd and 3rd trimesters, a change in the degree of VAD was registered in 78.2% of cases. Significant differences in postnatal clinical data were found in groups with absent, moderate and severe disproportion: no changes of the eventrated intestine were found in 50%, 34.1% and 7.1%, respectively, significant changes of the intestine were present in 12.5%, 36.4% and 50%, associated intestinal anomalies were diagnosed in 18.75%, 13.6% and 35.7%, primary correction with fascial closure was performed in 37.5%, 9.0% and 0%, staged repair with synthetic patch/silo and delayed abdominal wall closure in 0%, 20.5% and 57.1%. Mortality was 6.3%, 13.6% and 35.7%, respectively. Conclusions. A new method for assessing the congruence of the volumes of eventrated organs and abdominal cavity in fetuses with gastroschisis can provide important additional information for refining prenatal diagnosis, determining the severity of pathological process and predicting postnatal outcome. Prenatal evaluation of the degree of viscero-abdominal disproportion will allow to choose the correct management of pregnancy and labor, as well as to plan specialized care of the newborns. Key words: congenital malformations, prenatal diagnosis, anterior abdominal wall, gastroschisis, viscero-abdominal disproportion


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