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남매에서 발생한 C1q 신증 2례

Other Titles
 Two Cases of C1q Nephropathy in Siblings. 
Authors
 김수영  ;  김성헌  ;  문경철  ;  신재일  ;  정현주 
Citation
 Journal of the Korean Society of Pediatric Nephrology (대한소아신장학회지), Vol.16(1) : 46-50, 2012 
Journal Title
 Journal of the Korean Society of Pediatric Nephrology  (대한소아신장학회지) 
ISSN
 1226-5292 
Issue Date
2012
Abstract
C1q nephropathy is a distinct clinicopathologic entity, characterized by mesangial immunoglobulin and complement deposits, predominantly C1q, with no evidence for systemic lupus erythematosus. Clinically it may present as nephrotic syndrome and non-nephrotic proteinuria per se or associated with microscopic hematuria, gross hematuria, hypertension, or renal insufficiency. So far there is only one report about a familial case of C1q nephropathy (in two sisters). We present two cases of familial C1q nephropathy with nephrotic syndrome which was steroid resistant, but partially remitted with cyclosporine.
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DOI
10.3339/jkspn.2012.16.1.46
Appears in Collections:
1. Journal Papers (연구논문) > 1. College of Medicine (의과대학) > Dept. of Pediatrics (소아청소년과학교실)
1. Journal Papers (연구논문) > 1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실)
Yonsei Authors
신재일(Shin, Jae Il) ORCID logo https://orcid.org/0000-0003-2326-1820
정현주(Jeong, Hyeon Joo) ORCID logo https://orcid.org/0000-0002-9695-1227
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URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/92260
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