A5070947474- Renal Diseases and Glomerulopathies
- Vasculitis and related conditions
- Dialysis and Renal Disease Management
- Complement system in diseases
- Hemoglobinopathies and Related Disorders
- Platelet Disorders and Treatments
- Pediatric Urology and Nephrology Studies
- Systemic Lupus Erythematosus Research
- Iron Metabolism and Disorders
- Pulmonary Hypertension Research and Treatments
- Adolescent and Pediatric Healthcare
- Urological Disorders and Treatments
- Neonatal Health and Biochemistry
- Autoimmune and Inflammatory Disorders Research
- Inflammasome and immune disorders
- Renal Transplantation Outcomes and Treatments
- Parvovirus B19 Infection Studies
- Environmental and Sediment Control
- Kawasaki Disease and Coronary Complications
- Abdominal Trauma and Injuries
- Urticaria and Related Conditions
- Ocular Diseases and Behçet’s Syndrome
- HIV/AIDS drug development and treatment
- Hormonal and reproductive studies
- Trauma, Hemostasis, Coagulopathy, Resuscitation
Gaziantep University
2017-2024
Diyarbakır Askeri Hastanesi
2018-2022
ABSTRACT Background Two earthquakes on 6 February 2023 destroyed 10 cities in Türkiye. We report our experience with pediatric victims during these catastrophes, a focus crush syndrome related–acute kidney injury (Crush-AKI) and death. Method Web-based software was prepared. Patient demographics, time under rubble (TUR), admission laboratory data, dialysis, overall outcomes were recorded. Results A total of 903 injured children (median age 11.62 years) evaluated. Mean TUR 13 h (interquartile...
Abstract Background Acute post‐streptococcal glomerulonephritis ( APSGN ) is the most common post‐infectious in childhood. The aim of this study was therefore to identify possible risk factor(s) responsible for decreased glomerular filtration rate GFR . Methods data patients followed up with a diagnosis Pediatric Nephrology Clinic Gaziantep University Hospital between October 2014 and 2016 were retrospectively evaluated. Results total number subjects 75 (male/female, 42/33) mean age 8.20 ±...
Colorectal cancer is among the most common types in world and its etiology involves interaction of genetic environmental factors. ABCB1 highly expressed apical surface colonic epithelial cells acts as an efflux pump by transporting toxic endogenous substances, drugs xenobiotics out cells. polymorphisms may either change protein expression or alter function. Several studies have reported a possible association between variants colorectal cancer, but no consistent conclusion has been arrived...
This study aimed to evaluate the indications, complications, and outcomes of peritoneal dialysis (PD) in term neonates from a state hospital.The demographic, clinical, laboratory data 67 newborn infants who underwent PD within first 4 weeks life between June 2014 2019 were retrospectively analyzed.Twenty-five patients (37.3%) male, 42 (63.7%) female. The mean gestational age was 38.3 ± 0.8 (range: 37-40) birthweight 3,100 504.9 g 1,800-5,000 g). at start 7.97 8.34 days (range:1-44 days)...
Peritoneal dialysis (PD) is one of the most preferred kidney replacement therapies in children. However, it has an important complication such as peritonitis. This study was planned to investigate causes and frequency peritonitis children with PD.The demographic features, episodes, microbiological characteristics PD patients followed up for 5 years.Overall, 50 pediatric who met criteria a 5-year period were included study. Consanguineous marriage 64% 44% mothers illiterate. A total 19 had no...
Henoch-Schönlein purpura nephritis (HSN) is defined as with kidney involvement, including hematuria and/or proteinuria. The aim of this study was to evaluate the data HSN patients who underwent renal biopsy, and compare main clinical laboratory parameters that may affect biopsy findings, treatment protocols, short- long-term outcome those patients.Biopsies performed in 72 between January 2007 2017 were retrospectively evaluated. They divided into two groups according classification...
The objective of this study is to determine the clinical features unilateral multicystic dysplastic kidney (MCDK) patients.The demographic, clinical, laboratory, and radiologic MCDK patients at Diyarbakır Children’s Hospital Gazi Yaşargil Training Research between January 2008-June 2019 were retrospectively evaluated.A total 111 [59 (53.2%) male 52(46.8%) female] with followed for a mean period 41.89 ± 32.03 months. was located on left right sides in 46 (41.4%) 65 (58.6%) children,...
Background: Familial Mediterranean fever (FMF) is a hereditary autoinflammatory disorder commonly found in populations from the region, including Turks, Armenians, Arabs, and Jews. It characterized by recurrent episodes of inflammation, primarily affecting peritoneum, pleura, joints. caused mutations MEFV gene, which encodes pyrin, protein that regulates inflammatory response. The most common associated with FMF are M694V, M680I, V726A. These lead to overproduction interleukin-1β (IL-1β),...
Deferasirox is an iron chelator that used in B-thalassemia worldwide. Nephrotoxicity one of the common side effects deferasirox. can be seen form nephritis and tubulopathy. A 6-year-old male whose ferritin levels were above 3500 ng/mL reported this article. was increased from 30 mg/kg/day to 40 because high ferritin. In complete urinalysis patient after 3 weeks later +3 protein detected, spot urine protein/creatinine ratio 2.5. without symptoms findings, deferasirox discontinued. his...
Background To evaluate the demographic, clinical, laboratory findings, genetic results and final status of patients followed-up with diagnosis atypical hemolytic uremic syndrome (aHUS) Materials methods Patients who were diagnosed followed up in our pediatric nephrology center between January 2013 June 2021 included study retrospectively. Demographic data, history, age at diagnosis, physical examination, tests, organ involvement, results, treatments, renal replacement therapies, follow-up...
Abstract Background C3 glomerulopathy(C3G) is a complement-mediated disease caused by abnormalities in the alternative complement pathway. Although genetic studies are not required for diagnosis, they valuable treatment planning and prognosis prediction. The aim of this study to investigate clinical phenotypes, kidney survival, response MMF pediatric C3G patients with without mutations related genes. Methods Sixty were included, divided into two groups based on gene mutations. Demographic...
Atipik hemolitik üremik sendrom,
 alternatif komplemanın yolunun kronik kontrolsüz aktivasyonundan ortaya çıkan
 trombotik mikroanjiyopatinin nadir bir şeklidir. üremik
 sendrom, immün olmayan anemi, trombositopeni ve böbrek tutulumu ile
 ilişkilidir. Hastalık akut dönemde mortalite morbiditeye uzun son
 dönem yetmezliğine neden olabilir. Hastalıkta her ne kadar böbrek
 görülse de, vakaların % 20'sinde ekstra-renal tutulum görülebilir.
 Tanı konan...
ÖZ GİRİŞ ve AMAÇ: İzole pulmoner kapak yetersizliği (IPKY) nadir görülen bir klinik durumdur genellikle yıllarca iyi tolere edilir. IPKY'de sağ ventrikül diyastolik fonksiyonlarını değerlendirmek istedik
Aim: To report demographic, clinical and laboratory findings with outcome in childhood-onset systemic lupus erythematosus (cSLE)Material Methods: Charts of all children cSLE followed at pediatric rheumatology clinic Gaziantep University between 2000-2016 were reviewed. Demographic data, history, age diagnosis, physical examination, investigations, diagnostic criteria, follow-up duration therapeutic regimens noted. The adaptation the Systemic Lupus International Collaborating Clinics American...