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PMID: 4107267 Published · ppublish English Journal Article

Genetically determined heterogeneity of the C1 esterase inhibitor in patients with hereditary angioneurotic edema.

The Journal of clinical investigation ·Vol. 50 ·No. 10 ·1971-10-00 ·Pages 2143-9

Rosen FS, Alper CA, Pensky J, Klemperer MR, Donaldson VH

Abstract

Normal human serum contains 18 +/-5 mg/100 ml of C1 esterase inhibitor (alpha-2 neuraminoglycoprotein) as estimated by immunochemical means. Of 118 patients with hereditary angioneurotic edema, the sera of 80, from 42 kindred, contained a mean concentration of 3.15 mg/100 ml or 17.5% of normal. The mean serum concentration in 35 patients in 7 other kindred was 20 mg/100 ml or 111% of normal, and 3 patients in another kindred contained over 80 mg/100 ml or greater than 400% of normal. The nonfunctional inhibitors in patients' sera of these eight kindred were identical with normal C1 esterase inhibitor by Ouchterlony analysis, but they were different from normal and from each other with respect to their electrophoretic mobility, their capacity to bind C1 esterase, and their ability to inhibit esterolysis of N-acetyl-tyrosine-ethylester.

MeSH Terms
Acetates Alkanes Alpha-Globulins/analysis Angioedema/enzymology,genetics Animals Autoradiography Chromatography, Gel Complement System Proteins Electrophoresis Esterases/antagonists & inhibitors Esters Glycoproteins/blood Goats Humans Immunodiffusion Iodine Isotopes Metabolism, Inborn Errors/genetics Neuraminic Acids/blood Protein Binding Radioimmunoassay Tyrosine
Chemicals
Acetates Alkanes Alpha-Globulins Esters Glycoproteins Iodine Isotopes Neuraminic Acids Tyrosine Complement System Proteins Esterases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Rosen F S
Alper C A
Pensky J
Klemperer M R
Donaldson V H
References (14)
14 references, click to expand
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1971-10-00
Pages
2143-9
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC292148
Subset
IM
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