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Congenital X-linked hypogammaglobulinemia and asymptomatic hepatitis B antigen carrier state

  • Betty B. Wray
  • , Guy B. Faguet
  • , Henry M. Middleton
  • , Shyuan Hsia
  • , David T. Plaxico

Research output: Contribution to journalArticlepeer-review

Abstract

Hepatitis occurring in patients with congenital X-linked or common variable hypogammaglobulinemia has been reported to follow a usual pattern of rapid progression from acute hepatitis to either chronic active hepatitis or death. This article describes a 21-year-old black man with congenital X-linked hypogammaglobulinemia who has been known to be a hepatitis B-associated antigen carrier during a 9-year follow up period. Liver enzyme studies are normal. His immunologic studies demonstrate no impairment of cellular immunity. His brother, who has the same disease and lives in the same household, has remained negative for hepatitis B-associated antigen. This patient demonstrates that not all hypogammaglobulinemia patients invariably have a severe clinical course with hepatitis.

Original languageEnglish (US)
Pages (from-to)507-510
Number of pages4
JournalThe Journal of Allergy and Clinical Immunology
Volume76
Issue number3
DOIs
StatePublished - Sep 1985
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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