| Literature DB >> 1085610 |
J L McPhie, S Binnie, P W Brunt.
Abstract
Infantile liver disease with deficiency of serum alpha1-antitrypsin is illustrated by a description of the clinical, biochemical, and pathological findings in two affected families. The simplicity of the diagnostic tests is emphasized. Review of 61 biopsies of liver from children and adolescents provided a further 3 cases. It is prudent to exclude this metabolic defect in children with a history of "neonatal hepatitis".Entities:
Mesh:
Year: 1976 PMID: 1085610 PMCID: PMC1546112 DOI: 10.1136/adc.51.8.584
Source DB: PubMed Journal: Arch Dis Child ISSN: 0003-9888 Impact factor: 3.791