Article
[New therapeutic possibilities in alpha 1-antitrypsin deficiency].
Ugeskrift for laeger - 26 Mar 1990
Kok-Jensen A, Dirksen A, Evald T, Keittelmann S, Viskum K
Abstract excerpt
The alpha-1-antitrypsin gene is localized to chromosome 14. Numerous genetic variations may occur and some of these result in severely reduced concentration in the serum. The commonest cause of severe deficiency of alpha-1-antitrypsin is the gene-variant Z in the homozygotic form which occurs in...
Topics
- Female
- Genetic Counseling
- Genetic Engineering
- Heart-Lung Transplantation
- Humans
- Liver Transplantation
- Phenotype
- Pregnancy
- Prenatal Diagnosis
- alpha 1-Antitrypsin
- alpha 1-Antitrypsin Deficiency
