Literature DB >> 7271093

Lupus erythematosus-like syndrome with selective complete deficiency of C1q.

H Nishino, K Shibuya, Y Nishida, M Mushimoto.   

Abstract

A 37-year-old Japanese man in previously good health was hospitalized because of swelling of the auricles had discoid erythema of the face. Clinical and laboratory findings satisfied the diagnostic criteria for systemic lupus erythematosus proposed by the American Rheumatism Association. However, serologic studies showed weakly positive antinuclear factor and absence of anti-DNA antibody and lupus erythematosus cells. A striking abnormality was the total absence of serum hemolytic complement activity (CH50). Further studies showed selective complete deficiency of C1q, a subunit of the first component of complement (C1). This is the first reported case of lupus erythematosus-like syndrome with selective complete deficiency of C1q.

Entities:  

Mesh:

Year:  1981        PMID: 7271093     DOI: 10.7326/0003-4819-95-3-322

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


  16 in total

Review 1.  Genetic susceptibility to lupus: the biological basis of genetic risk found in B cell signaling pathways.

Authors:  Samuel E Vaughn; Leah C Kottyan; Melissa E Munroe; John B Harley
Journal:  J Leukoc Biol       Date:  2012-06-29       Impact factor: 4.962

2.  Genetic factors predisposing to systemic lupus erythematosus and lupus nephritis.

Authors:  Paula S Ramos; Elisabeth E Brown; Robert P Kimberly; Carl D Langefeld
Journal:  Semin Nephrol       Date:  2010-03       Impact factor: 5.299

Review 3.  Genetics of Sjögren's syndrome in the genome-wide association era.

Authors:  John A Ice; He Li; Indra Adrianto; Paul Chee Lin; Jennifer A Kelly; Courtney G Montgomery; Christopher J Lessard; Kathy L Moser
Journal:  J Autoimmun       Date:  2012-01-29       Impact factor: 7.094

Review 4.  Lupus diseases associated with hereditary and acquired deficiencies of complement.

Authors:  V Agnello
Journal:  Springer Semin Immunopathol       Date:  1986

5.  A homozygous point mutation results in a stop codon in the C1q B-chain of a C1q-deficient individual.

Authors:  R A McAdam; D Goundis; K B Reid
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

Review 6.  C1q as an autocrine and paracrine regulator of cellular functions.

Authors:  Berhane Ghebrehiwet; Kinga H Hosszu; Ellinor I B Peerschke
Journal:  Mol Immunol       Date:  2016-11-30       Impact factor: 4.407

Review 7.  Clinical perspectives on lupus genetics: advances and opportunities.

Authors:  Judith A James
Journal:  Rheum Dis Clin North Am       Date:  2014-06-10       Impact factor: 2.670

8.  SLE like syndrome and functional deficiency of C1q in members of a large family.

Authors:  A J Hannema; J C Kluin-Nelemans; C E Hack; A J Eerenberg-Belmer; C Mallée; H P van Helden
Journal:  Clin Exp Immunol       Date:  1984-01       Impact factor: 4.330

9.  Sex Differences in monocytes and TLR4 associated immune responses; implications for systemic lupus erythematosus (SLE).

Authors:  Wei Jiang; Gary Gilkeson
Journal:  J Immunother Appl       Date:  2014-03-07

Review 10.  Complement and systemic lupus erythematosus.

Authors:  Mark J Walport
Journal:  Arthritis Res       Date:  2002-05-09
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.