Alpha-1-antitrypsin (Pi) types in Down's syndrome

Clin Genet. 1976 Oct;10(4):239-43. doi: 10.1111/j.1399-0004.1976.tb00041.x.

Abstract

Alpha-1-antitrypsin (Pi) phenotypes have been determined in 40 patients suffering from Down's syndrome. Thirty-six of the patients were found to have a normal M phenotype, whereas two deficient phenotypes of the MS variety were observed. In addition, two M variants were noted. The significance of an M variant phenotype in some patients with Down's syndrome is not completely understood and is currently under investigation. Since the majority of the patients had a normal alpha-1-antitrypsin phenotype, the results of this study indicate that a deficiency in alpha-1-antitrypsin plays no role in the respiratory fragility of individuals with Down's syndrome.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Down Syndrome / genetics*
  • Female
  • Genetic Variation
  • Humans
  • Infant
  • Male
  • Phenotype
  • alpha 1-Antitrypsin* / analysis

Substances

  • alpha 1-Antitrypsin