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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
Keywords
C1q nephropathy ; Nephrotic syndrome ; Steroid resistant
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.
Files in This Item:
T201203364.pdf Download
DOI
10.3339/jkspn.2012.16.1.46
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아과학교실) > 1. Journal Papers
Yonsei Authors
Shin, Jae Il(신재일) ORCID logo https://orcid.org/0000-0003-2326-1820
Jeong, Hyeon Joo(정현주) ORCID logo https://orcid.org/0000-0002-9695-1227
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/92260
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