Literature DB >> 6848983

Inherited deficiency of the third component of complement associated with recurrent pyogenic infections, circulating immune complexes, and vasculitis in a Dutch family.

J J Roord, M Daha, W Kuis, H A Verbrugh, J Verhoef, B J Zegers, J W Stoop.   

Abstract

A family is described in which 3/11 children showed a homozygous deficiency of C3, and both parents and six other children had subnormal levels of C3. The three children with selective C3 deficiency suffered repeatedly from bacterial infections, whereas the parents and the other siblings were clinically healthy. During infectious episodes the patients showed a maculopapular skin rash, and at such times immune complexes were present in the serum. Biopsy specimens of the skin lesions showed the picture of leukocytoclastic vasculitis.

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Year:  1983        PMID: 6848983

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  15 in total

1.  Homozygous hereditary C3 deficiency due to a premature stop codon.

Authors:  Edimara Da Silva Reis; Gisele Vanessa Baracho; Adriana Sousa Lima; Chuck S Farah; Lourdes Isaac
Journal:  J Clin Immunol       Date:  2002-11       Impact factor: 8.317

2.  The inaccessibility of the outer membrane of adherent Treponema pallidum (Nichols strain) to anti-treponemal antibodies, a possible role of serum proteins.

Authors:  J J van der Sluis; M Kant; P C Onvlee; E Stolz
Journal:  Genitourin Med       Date:  1990-06

3.  Human complement component C3: cDNA coding sequence and derived primary structure.

Authors:  M H de Bruijn; G H Fey
Journal:  Proc Natl Acad Sci U S A       Date:  1985-02       Impact factor: 11.205

4.  Surface hydrophobicity and opsonic requirements of coagulase-negative staphylococci in suspension and adhering to a polymer substratum.

Authors:  A Pascual; A Fleer; N A Westerdaal; M Berghuis; J Verhoef
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1988-04       Impact factor: 3.267

5.  Analysis of C3-receptor activity on human B-lymphocytes and isolation of the complement receptor type 2 (CR2).

Authors:  K J Micklem; R B Sim; E Sim
Journal:  Biochem J       Date:  1984-11-15       Impact factor: 3.857

6.  Functional deficiency of complement factor D in a monozygous twin.

Authors:  H C Kluin-Nelemans; H van Velzen-Blad; H P van Helden; M R Daha
Journal:  Clin Exp Immunol       Date:  1984-12       Impact factor: 4.330

7.  Molecular basis of hereditary C3 deficiency.

Authors:  M Botto; K Y Fong; A K So; A Rudge; M J Walport
Journal:  J Clin Invest       Date:  1990-10       Impact factor: 14.808

8.  An association between homozygous C3 deficiency and low levels of anti-pneumococcal capsular polysaccharide antibodies.

Authors:  M A Hazlewood; D S Kumararatne; A D Webster; M Goodall; P Bird; M Daha
Journal:  Clin Exp Immunol       Date:  1992-03       Impact factor: 4.330

9.  Homozygous hereditary C3 deficiency due to a partial gene deletion.

Authors:  M Botto; K Y Fong; A K So; R Barlow; R Routier; B J Morley; M J Walport
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-01       Impact factor: 11.205

10.  Deficiency of complement component C3 is associated with accelerated removal of soluble 123I-labelled aggregates of IgG from the circulation.

Authors:  C Halma; M R Daha; J A Camps; J H Evers-Schouten; E K Pauwels; E s Van
Journal:  Clin Exp Immunol       Date:  1992-12       Impact factor: 4.330

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