THIS familial syndrome of eczema, thrombocytopenia and recurrent infection was described by Wiskott1 in 1937, but it was not until 1954 that Aldrich, Steinberg and Campbell2 defined it as a sex-linked recessive disease. The majority of children afflicted with this baffling disorder have died as a result of overwhelming bacterial infection. Recently, however, visceral invasion by measles virus and cytomegalovirus has been described as an additional microbial complication.3 In our own hospital, within a period of two and a half years, we observed an alarming progression of primary herpetic gingivostomatitis in 3 boys with this syndrome. Two of these patients . . .
No takes yet. Share an insight, caveat, or question.
Geme et al. (1965) studied this question.
Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context: