vesico-ureteral reflux/obesity

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10 rezultatet

The impact of obesity on febrile urinary tract infection and renal scarring in children with vesicoureteral reflux.

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Identifikohuni Regjistrohu

BACKGROUND It has become clear that obesity is associated with a variety of infectious diseases, including urinary tract infection (UTI) and renal scarring. OBJECTIVE The aim of this study was to evaluate the association between obesity and the degree of febrile UTI (fUTI) and renal scarring in

Weight Gain and Obesity in Infants and Young Children Exposed to Prolonged Antibiotic Prophylaxis.

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Identifikohuni Regjistrohu

UNASSIGNED An association between antibiotic use and excessive weight gain or obesity in healthy infants and young children has been reported, but evidence is inconsistent and based on observational studies of growth in relation to incidental antibiotic exposures. UNASSIGNED To evaluate whether

Predictors of becoming overweight among pediatric patients at risk for urinary tract infections.

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Identifikohuni Regjistrohu

BACKGROUND The association between obesity and urinary dysfunction in childhood has been described, albeit through retrospective analysis, making temporal relationships difficult to establish. OBJECTIVE The objective of this study was to determine risk factors for significant weight gain in children

Gender, degree of obesity, and discrepancy between urea and creatinine clearance in peritoneal dialysis.

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Identifikohuni Regjistrohu

The effect of gender and degree of obesity on the size indicators V, used to normalize urea clearance (Kt/Vur), and body surface area (BSA), used to normalize creatinine clearance (Ccr), in peritoneal dialysis was studied by: (1) mathematical comparison of the formulae used to estimate V (Watson and

Nephrotic proteinuria without hypoalbuminemia: clinical characteristics and response to angiotensin-converting enzyme inhibition.

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Identifikohuni Regjistrohu

Although hypoalbuminemia is a fundamental characteristic of nephrotic syndrome (NS), there are many patients with massive proteinuria that do not develop hypoalbuminemia. We have studied the clinical and biochemical characteristics of 19 patients with persistent massive proteinuria (greater than 5

Absence of hypoalbuminemia despite massive proteinuria in focal segmental glomerulosclerosis secondary to hyperfiltration.

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Identifikohuni Regjistrohu

We observed that some patients do not develop hypoalbuminemia despite the presence of massive proteinuria. To investigate whether the absence or presence of hypoalbuminemia could be a marker in the distinction between idiopathic focal segmental glomerulosclerosis (FSG) and FSG secondary to

[Prader-Willi syndrome associated with chromosomal aberration: report of a case].

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Identifikohuni Regjistrohu

A male case of Prader-Willi syndrome (2.8 years in age) with an interstitial deletion of a chromosome affecting 15q 11-12 region is reported. The chief complaints were hypoplastic scrotum and defect of bilateral scrotal content. The clinical features were short stature, obesity, delayed mental

Fat, demented and stupid: An unrecognized legacy of pediatric urology?

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Identifikohuni Regjistrohu

The human body is an unfathomably intricate structure consisting of many connected and intertwined systems. This makes it impossible for therapeutic interventions to selectively target only one physiologic system without some impact or side effects on all the other systems. The resiliency of the

Psychosocial and respiratory disease related to severe bladder dysfunction and non-monosymptomatic enuresis.

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Identifikohuni Regjistrohu

OBJECTIVE Complicated bladder dysfunctions (BD) (associated with infections/urological complications or irresponsive to treatment) are a small proportion of all cases, but are highly morbid, clinically and psychosocially. Our aim is to describe a cohort of complicated pediatric BD, using subgroup

Maternal risk factors involved in specific congenital anomalies of the kidney and urinary tract: A case-control study.

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Identifikohuni Regjistrohu

BACKGROUND Congenital anomalies of the kidney and urinary tract (CAKUT) comprise a heterogeneous group of birth defects with a variety of genetic and nongenetic factors suspected of involvement in the etiology. However, little is known about risk factors in specific CAKUT phenotypes. Therefore, we

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