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Published on: February 20, 2015
Kidney function tests in children with beta-thalassemia minor in Zahedan, southeast of Iran
Simin Sadeghi-Bojd1, Mohammad Hashemi, Majid Naderi
1Department of Pediatrics, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran. sisadegh@yahoo.com
Insights
Children with beta-thalassemia minor show signs of kidney tubule issues, including protein and beta2-microglobulin in urine. Further research is needed to understand this link between beta-thalassemia minor and renal tubular dysfunction.
Area of Science:
- Nephrology
- Pediatrics
- Hematology
Background:
- Beta-thalassemia minor is a common genetic blood disorder.
- Limited data exists on kidney function in individuals with beta-thalassemia minor.
Purpose of the Study:
- To investigate kidney function in children diagnosed with beta-thalassemia minor.
- To identify potential renal tubular abnormalities associated with this condition.
Main Methods:
- Collected 24-hour urine samples from 50 children with beta-thalassemia minor for analysis.
- Analyzed urine for electrolytes, creatinine, protein, and beta2-microglobulin.
- Performed blood tests for hematologic and biochemical parameters, including kidney function markers.
Main Results:
- Prevalence of proteinuria was 32%, beta2-microglobulinuria was 36%, calciuria was 4%, phosphaturia was 4%, and uricosuria was 20%.
- These findings suggest evidence of renal tubulopathy in the studied pediatric cohort.
- Observed abnormalities indicate potential renal tubular dysfunction.
Conclusions:
- The study supports the presence of renal tubular dysfunction in children with beta-thalassemia minor.
- Further large-scale studies are recommended to elucidate the relationship between beta-thalassemia minor and renal dysfunction.
Abstract:
There is little information regarding kidney function in patients with beta-thalassemia minor. In this study we investigated kidney function tests in 50 children with beta-thalassemia minor (22 boys and 28 girls). Twenty-four-hour urine samples were collected and analyzed for sodium, potassium, calcium, magnesium, creatinine, phosphate, uric acid, protein, and beta2-microglobulin. Blood samples were obtained for hematologic and biochemical analyses including complete blood count, serum ferritin, sodium, potassium, calcium, phosphate, magnesium, creatinine, and uric acid. This group of children with beta-thalassemia showed some evidence of tubulopathy such as proteinuria (32%), beta2-microglobulin excretion (36%), calciuria (4%), phosphaturia (4%), and uricosuria (20%). Our findings support the existence of renal tubular dysfunction in beta-thalassemia minor. However, further studies in large series are needed to shed light on the possible relation of these two distinct diseases.
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