| Autor: |
M. R. Baiocchi, E. Manzato, G. Crepaldi, C. Lista, S. Pauluzzi, F. Fabiani, R. Fellin, G. Baldo, G. Baggio |
| Rok vydání: |
1983 |
| Předmět: |
|
| Zdroj: |
Atherosclerosis VI ISBN: 9783642818196 |
| DOI: |
10.1007/978-3-642-81817-2_17 |
| Popis: |
Analbuminemia or better hypoalbuminemia is a rare disease, first described in 1954 by Bennhold et al. (1), and is characterized by the almost total absence of albumin. This disease is inherited and is probably transmitted by a recessive autosomal gene (2,3). The defect is not complete. The albumin traces present in circulation on Immunoelectrophoresis show the same mobility as normal albumin (4) and no antigenic differences between normal albumin and that in subjects with analbuminemia have been detected (5). In this desease an increased catabolism or loss of this protein may also be ruled out: perfusion of albumin labelled with radioactive iodine has in fact shown a remarkable increase in the half-life of albumin (6,7). |
| Databáze: |
OpenAIRE |
| Externí odkaz: |
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