| Hyper IgM syndrome and complement Clq deficiency in an individual with systemic lupus erythematosus-like disease. | |
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MedLine Citation:
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PMID: 20810037 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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Many immunedeficiency syndromes are associated with autoimmune disorders. We here report on a girl with a systemic lupus erythematosus-like disease who suffered from both hyperimmunoglobulin M syndrome (HIGMS) and C1q deficiency. Despite severe central nervous system-lupus like disease, probably due to C1q deficiency, kidney function was relatively spared. IgM autoantibody might play a protective role against lupus-glomerulonephritis. |
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Authors:
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I Tsuge; Y Kondo; Y Nakajima; N Nakagawa; K Imai; S Nonoyama; K Oshima; O Ohara; M Hatanaka; E Kitano; H Kitamura; A Urisu |
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Publication Detail:
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Type: Case Reports; Journal Article Date: 2010-08-30 |
Journal Detail:
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Title: Clinical and experimental rheumatology Volume: 28 ISSN: 0392-856X ISO Abbreviation: Clin. Exp. Rheumatol. Publication Date: 2010 Jul-Aug |
Date Detail:
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Created Date: 2010-09-02 Completed Date: 2010-12-02 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 8308521 Medline TA: Clin Exp Rheumatol Country: Italy |
Other Details:
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Languages: eng Pagination: 558-60 Citation Subset: IM |
Affiliation:
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Department of Paediatrics, Fujita Health University, Aichi, Japan. itsuge@fujita-hu.ac.jp |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Child Complement C1q / deficiency* Female Humans Hyper-IgM Immunodeficiency Syndrome / complications*, diagnosis Immunoglobulin M / physiology Lupus Erythematosus, Systemic / complications, diagnosis, etiology* Lupus Nephritis / physiopathology, prevention & control |
| Chemical | |
Reg. No./Substance:
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0/Immunoglobulin M; 80295-33-6/Complement C1q |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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