Document Detail


The natural history of liver disease in alpha 1-antitrypsin deficient children.
MedLine Citation:
PMID:  2905108     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
During 1972-1974, 200,000 Swedish infants were screened for alpha 1-antitrypsin deficiency. Of 127 PiZ (Protease inhibitor) children followed from infancy to 12 years of age, four PiZ children with neonatal liver disease have died; two of liver cirrhosis, one was found to have liver cirrhosis at autopsy, having died of aplastic anemia and the fourth died in an accident. Liver microscopy showed a mild increase of periportal fibrous tissue. Another PiZ child died of anaphylactic shock. At 12 years of age, none of the PiZ children have clinical symptoms of liver disease. No PiZ-, PiSZ, PiS- or PiFZ child has had any clinical symptom of liver disease. One PiSZ child died of sudden infant death syndrome. Laboratory analyses from birth through 12 years of age have shown increased S-Bilirubin levels in 11% of the PiZ infants, which normalized within the first half year of life. S-GT was abnormal in about half of the infants, but had normalized when checked at 8 and 12 years of age in all but 6-3% of the PiZ children. The percentage of abnormal S-ALAT test results have decreased from 73% during the first year of life, to about 15% at the age of 12. The range of the abnormal levels also decreased considerably. Abnormal S-GT or S-ALAT levels were found in about 20% of the PiSZ infants, the proportion decreasing to 2% at the age of 12.
Authors:
T Sveger
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Acta paediatrica Scandinavica     Volume:  77     ISSN:  0001-656X     ISO Abbreviation:  Acta Paediatr Scand     Publication Date:  1988 Nov 
Date Detail:
Created Date:  1989-02-02     Completed Date:  1989-02-02     Revised Date:  2009-11-11    
Medline Journal Info:
Nlm Unique ID:  0000211     Medline TA:  Acta Paediatr Scand     Country:  SWEDEN    
Other Details:
Languages:  eng     Pagination:  847-51     Citation Subset:  IM    
Affiliation:
Department of Pediatrics, University of Lund, Malmö General Hospital, Sweden.
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MeSH Terms
Descriptor/Qualifier:
Alanine Transaminase / blood
Child
Child, Preschool
Humans
Infant
Infant, Newborn
Liver Diseases / enzymology,  etiology*
Phenotype
Prospective Studies
alpha 1-Antitrypsin Deficiency*
gamma-Glutamyltransferase / blood
Chemical
Reg. No./Substance:
EC 2.3.2.2/gamma-Glutamyltransferase; EC 2.6.1.2/Alanine Transaminase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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