Congenital Deficiency of C2 and Factor B
- 7 December 1978
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 299 (23) , 1313
- https://doi.org/10.1056/nejm197812072992316
Abstract
To the Editor: Recently, Newman et al.1 reported decreased levels of properdin factor B in three homozygous C2-deficient children, an association attributed to the linkage between genes coding for the two proteins. The authors cite the papers by Glass2 and Raum3 and their colleagues as in agreement. In the paper by Glass et al.2 the only person with homozygous C2 deficiency, a patient with systemic lupus erythematosus, had a factor B level of 320 μg per milliliter, which was within the normal range. This paper reported a statistical difference in factor B levels between heterozygous C2-deficient and normal family members . . .Keywords
This publication has 4 references indexed in Scilit:
- Recurrent Septicemia Associated with Congenital Deficiency of C2 and Partial Deficiency of Factor B and the Alternative Complement PathwayNew England Journal of Medicine, 1978
- The chromosomal order of genes controlling the major histocompatibility complex, properdin factor B, and deficiency of the second component of complement.Journal of Clinical Investigation, 1976
- Inherited structural polymorphism in human C2: evidence for genetic linkage between C2 and Bf.The Journal of Experimental Medicine, 1976
- Inherited deficiency of the second component of complement. Rheumatic disease associations.Journal of Clinical Investigation, 1976