Modification of the alpha 1-antitrypsin phenotype in neonatal hepatitis

Arch Dis Child. 1985 Apr;60(4):378-9. doi: 10.1136/adc.60.4.378.

Abstract

Two cases of neonatal hepatitis are described, one related to cytomegalovirus infection and the other idiopathic. In both infants a transient abnormality of the alpha 1-antitrypsin phenotype, inconsistent with the parent's phenotypes, reverted to normal during the convalescent phase of the illness.

Publication types

  • Case Reports

MeSH terms

  • Female
  • Hepatitis / blood
  • Hepatitis / genetics*
  • Humans
  • Infant, Newborn
  • Infant, Premature, Diseases / blood
  • Infant, Premature, Diseases / genetics*
  • Male
  • Phenotype
  • alpha 1-Antitrypsin Deficiency*