Alpha-1-antitrypsin (AAT) deficiency is a rare genetic disorder characterized by hepatitis in neonates, childhood and adulthood (protease inhibitor (PI)\*ZZ) and emphysema with or without hepatitis (PI\*ZZ)/(PI\*SS,SZ or null) in adulthood. We report the case of a female neonate born at 40Β weeks of
β¦ LIBER β¦
Rapid EM diagnosis in cases of Reye's syndrome and alpha-1-antitrypsin deficiency
β Scribed by Koert P. Dingemans; Marius A. van den Bergh Weerman
- Book ID
- 108014944
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 622 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0739-6260
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