α-Antitrypsin Deficiency and Neonatal Hepatitis

Five out of 28 infants investigated in a regional survey of neonatal hepatitis were found to have genetically-determined deficiency of α(1)-antitrypsin (ZZ phenotype). The clinical course and pathological changes varied considerably. All five infants had an acute hepatitis-like illness, and although...

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Bibliographic Details
Main Authors: Porter, C. A., Mowat, Alex P., Cook, P. J. L., Haynes, D. W. G., Shilkin, K. B., Williams, Roger
Format: Artigo
Language:Inglês
Published: 1972
Subjects:
Papers and Originals
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1785986/
https://ncbi.nlm.nih.gov/pubmed/5069219
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