Abstract
Primary X-linked (Bruton's) hypogammaglobulinaemia is uncommon. It usually presents clinically within the first two years of life — Typically after the age of three months when maternal IgG is exhausted.1 Its diagnosis in middle life is exceptional. The presentation of the condition as a triple infection in a middle-aged man therefore seemed worthwhile reporting, as effective and safe prophylactic immunotherapy is now available.
Get full access to this article
View all access options for this article.
References
1.
Webster
ADB
. Immune deficiency . Oxford Textbook of Medicine
1987 ; 1 ;475 –477 .
2.
Yap
PL
. The use of intravenous immunoglobulin for the treatment of infection; an overview . J of Infection
1987 ; 15 ; 21 –28 .
3.
Wolfe
MS
. Giardiasis . N Eng J Med
1978 ; 298 : 319 –321 .
4.
Bodey
GP
Fanistein
V
Guerrant
R.
Infections of the gastro-intestinal tract in the immunocompromised patient . Ann Rev Med
1986 ; 37 : 271 –281 .
5.
Leen
GLS
Birch
ADJ
Brettle
RP
Welsby
PD
Yap
PL
. Salmonella in patients with primary hypogammaglobulinaemia . J of Infection
1986 ; 12 ;241 –245 .
6.
Liodna
C
McNulty
AM
. Campylobacter pyloritis — Associated gastritis . J of Infection
1986 ; 13 ;107 –113 .
