نتایج جستجو برای: urinary tract anomalies
تعداد نتایج: 250990 فیلتر نتایج به سال:
The field of prenatal diagnosis of congenital anomalies has had great advances in recent years. Today we are able to diagnose different fetal anomalies in early developmental stages, and correct some of them, through prenatal fetal surgery. In this paper, we begin by describing the advances in surgical treatment of some fetal diseases such as, diaphragmatic hernia, lung sequestration, pleural e...
Submit Manuscript | http://medcraveonline.com Abbreviations: AMH: Anti-Mullerian Hormone; AR: Androgen Receptors; ATF3: Activating Transcription Factor 3; CPAs: Congenital Penile Anomalies; CWH: Chordee Without Hypospadias; EDCs: Endocrine Disrupting Chemicals; KFS: Klinefelter Syndrome; LUTS: Lower Urinary Tract Symptoms; MAGPI: Meatal Advancement and Glanuloplasty Incorporated; SMR: Split Med...
ABSTRACT Congenital genitourinary tract abnormalities occur in 0.1% to 1% of all neonates and are a major cause of perinatal mortality and morbidity. Nowadays, prenatal ultrasonography can detect most malformations and anomalies. In this study the genitourinary tract abnormalities of the Fetuses of the pregnant women by prenatal ultrasonography and causes of these abnormalities were evaluated...
Objective: Prune-belly syndrome is a rare congenital disorder characterized by musculature deficiency in the abdominal wall, lower urinary tract obstruction, other urinary tract anomalies, and bilateral cryptorchidism. The syndrome is commonly associated with pulmonary, skeletal, cardiac, and gastrointestinal defects. Over 95% of patients are male. Urinary tract disease is the major prognostic ...
The definition of congenital anomalies of the kidney and urinary tract (CAKUT) is the disease of structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux (VUR). These anomalies can cause pediatric chronic kidney disease. However, the pathogenesis of CAKUT is not well understood, because identifying the genetic architecture of CAKUT is difficult due to the phe...
Congenital anomalies of the kidney and urinary tract (CAKUT) form a group of heterogeneous disorders that affect the kidneys, ureters and bladder, with frequent asynchronous presentations and multiple CAKUT associations in the same individual. Urinary tract formation is a complex process, dependent of the interaction of multiple genes and their sub-product. The same genic alterations can lead t...
Urethral polyps are a rare finding in children. Urethral fibroepithelial polyps are usually discovered in the first decade of life. They present with voiding dysfunction, obstructive and irritative urinary symptoms, and hematuria. They may be associated with other congenital urinary tract anomalies. Histopathologically, they are usually benign lesions with no tendency to recurrence and are trea...
A 4-week-old boy with previous urinary tract infection and documented vesicoureteral reflux presented with urosepsis and septic arthritis of the right hip. Compliance with prophylactic antibiotic therapy had been poor at home. Complications such as bone and joint infection are known to occur after urinary tract infection in children with urologic abnormalities. However, previous similar reports...
Between 1990-97 two hundered children referred to our department with end-stage renal disease (ESRD) for renal replacement therapy. The ages of these children were 1-14 years (mean 8.14). There was no significant difference in incidence of ESRD between two sexes. We evaluated these children for the causes of ESRD. The most common causes were: Pylonephritis and congenital anomalies of urinary tr...
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