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Dense deposit disease in Korean children: a multicenter clinicopathologic study
Se Jin Park1, Yong-Jin Kim, Tae-Sun Ha
1Department of Pediatrics, Ajou University Hospital, Ajou University School of Medicine, Suwon, Korea.
This study reveals distinct clinical and pathological features of dense deposit disease (DDD) in Korean children compared to American children. Korean children exhibit milder kidney disease symptoms and specific glomerular basement membrane changes.
Area of Science:
- Pediatric Nephrology
- Glomerular Diseases
- Renal Pathology
Background:
- Dense deposit disease (DDD) is a rare kidney disorder.
- Understanding ethnic variations in DDD presentation is crucial for diagnosis and management.
Purpose of the Study:
- To investigate the clinical, laboratory, and pathologic characteristics of DDD in Korean children.
- To compare these characteristics with those of American children with DDD.
Main Methods:
- A structured protocol was distributed to pediatric nephrologists in Korea.
- Data from Korean children were compared with published data on American children with DDD.
- Clinical, laboratory, light microscopy, and electron microscopy findings were analyzed.
Main Results:
- Korean children showed lower proteinuria and higher serum albumin levels than American children.
- Membranoproliferative glomerulonephritis patterns were more common in Korean children (77.8%) versus American children (28.6%).
- Crescents were prevalent in American children (78.6%) but absent in Korean children; segmental electron dense deposits were more frequent in Korean children (100%).
Conclusions:
- Korean children with DDD present with milder proteinuria and hypoalbuminemia.
- Distinct histological patterns, including membranoproliferative glomerulonephritis and electron dense deposit location, differentiate Korean and American pediatric DDD cases.
- These findings highlight ethnic variations in DDD pathology.
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