10 results match your criteria: "Bursa Dörtçelik Pediatric Hospital[Affiliation]"

Evaluation of renal elasticity by shear wave elastography in children with Familial Mediterranean Fever.

Pediatr Nephrol

January 2025

Department of Radiology, Bursa Yuksek Ihtisas Egitim Ve Arastirma Hastanesi, Bursa, Turkey.

Background: Familial Mediterranean Fever (FMF) is a genetic disorder that can cause kidney damage. Shear wave elastography (SWE), a non-invasive method, was used to evaluate the decrease in renal tissue elasticity as a predictive parameter for amyloidosis. This study aimed to examine the changes in renal elasticity in patients with FMF using the renal SWE measurement method.

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Our knowledge of the factors related to parenting styles affecting adherence to diet in children with celiac diseases (CDs) and the association between psychiatric difficulties and diet compliance is largely based on limited data. Therefore, our work aims to examine primarily coexisting psychiatric difficulties in children with CD and raising attitudes of their parents and secondarily the relationship among adherence to treatment, psychiatric difficulties, and parental attitudes. Children aged 4-12 years (n = 42) who have been followed up with the diagnosis of CD in a Paediatric Gastroenterology Outpatient Clinic were compared with those of healthy controls (n = 31).

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Background: Catheter-Associated Urinary Tract Infections (CAUTIs) frequently occur in the intensive care unit (ICU) and are correlated with a significant burden.

Methods: We implemented a strategy involving a 9-element bundle, education, surveillance of CAUTI rates and clinical outcomes, monitoring compliance with bundle components, feedback of CAUTI rates and performance feedback. This was executed in 299 ICUs across 32 low- and middle-income countries.

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Simple Measurement of IgA Predicts Immunity and Mortality in Ataxia-Telangiectasia.

J Clin Immunol

November 2021

Division of Allergology, Pulmonology and Cystic Fibrosis, Department for Children and Adolescents, Goethe University, Frankfurt, Germany.

Article Synopsis
  • - Patients with ataxia-telangiectasia (A-T) often experience severe issues, including progressive coordination problems, weakened immune response, and higher cancer risk, with those having IgA deficiency facing even worse outcomes.
  • - A study of 659 A-T patients showed that those with IgA deficiency had significantly lower lymphocyte counts and altered immune cell types compared to those without IgA deficiency, indicating poorer health.
  • - The findings suggest that IgA deficiency serves as a simple indicator of worse prognosis in A-T patients, emphasizing the need for careful monitoring and potential treatment strategies for those affected.
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Aims: Pandemics can cause substantial psychological distress; however, we do not know the impact of the COVID-19 related lockdown and mental health burden on the parents of school age children. We aimed to comparatively examine the COVID-19 related the stress and psychological burden of the parents with different occupational, locational, and mental health status related backgrounds.

Methods: A large-scale multicenter online survey was completed by the parents ( = 3,278) of children aged 6 to 18 years, parents with different occupational (health care workers-HCW [18.

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Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome.

J Exp Med

September 2015

St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY 10065 Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM U1163, Necker Enfants Malades Hospital, 75015 Paris, France University Paris Descartes, Imagine Institute, 75006 Paris, France

Article Synopsis
  • Autosomal recessive TYK2 deficiency can lead to increased susceptibility to bacterial and viral infections, with varying symptoms among affected individuals.
  • Eight patients from different ethnicities were studied, revealing that while they all faced infections due to impaired immune responses, none exhibited the full hyper-IgE syndrome features seen in the first patient described.
  • The core issue in TYK2 deficiency is the inability to effectively respond to certain interleukins (IL-12 and IFN-α/β), which causes the infections, but the lack of HIES symptoms suggests that impaired IL-6 responses are not a fundamental aspect of this deficiency.
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The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.

J Allergy Clin Immunol

August 2015

Department of Immunology and Molecular Pathology, Royal Free Hospital and University College London, London, United Kingdom; Center for Chronic Immunodeficiency (CCI), University Medical Center Freiburg, Freiburg, Germany. Electronic address:

Background: Mutations in dedicator of cytokinesis 8 (DOCK8) cause a combined immunodeficiency (CID) also classified as autosomal recessive (AR) hyper-IgE syndrome (HIES). Recognizing patients with CID/HIES is of clinical importance because of the difference in prognosis and management.

Objectives: We sought to define the clinical features that distinguish DOCK8 deficiency from other forms of HIES and CIDs, study the mutational spectrum of DOCK8 deficiency, and report on the frequency of specific clinical findings.

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Objectives: The extent and relevance of altered bone metabolism for statural growth in children with chronic kidney disease is controversial. We analyzed the impact of renal dysfunction and recombinant growth hormone therapy on a panel of serum markers of bone metabolism in a large pediatric chronic kidney disease cohort.

Methods: Bone alkaline phosphatase (BAP), tartrate-resistant acid phosphatase 5b (TRAP5b), sclerostin and C-terminal FGF-23 (cFGF23) normalized for age and sex were analyzed in 556 children aged 6-18 years with an estimated glomerular filtration rate (eGFR) of 10-60 ml/min/1.

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Background/aims: Data about the efficiency and outcome of therapeutic endoscopic techniques in children with nonvariceal upper gastrointestinal bleeding (UGB) are scarce. We aimed to analyze our experience with endoscopic hemoclip application in children with non-variceal UGB.

Materials And Methods: During a 3-year period, a total of 1715 endoscopies were performed in our pediatric endoscopy unit; 182 (10.

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Liver involvement in children with Familial Mediterranean fever.

Dig Liver Dis

August 2012

Department of Pediatric Gastroenterology, Hepatology and Nutrition, Dörtçelik Pediatric Hospital, Bursa, Turkey.

Aim: Familial Mediterranean fever is characterised by recurrent, febrile, inflammatory attacks of the serosal membranes. Prolonged inflammatory response is triggered secondary to cytokine stimulation due to reduced activity of pyrin. Inflammatory cytokines play major role in the pathogenesis of acute liver injury; and chronic, recurrent cytokine production may cause chronic hepatitis/cirrhosis.

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