FREE NEJM E-TOC    HOME   |   SUBSCRIBE   |   CURRENT ISSUE   |   PAST ISSUES   |   COLLECTIONS   |   Search Term  Advanced Search

Sign in | Get NEJM's E-Mail Table of Contents — Free | Subscribe

Previous Volume 335:1523-1525 November 14, 1996 Number 20 Next

	Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.

	Full Text Purchase this article Add to Personal Archive Add to Citation Manager Notify a Friend E-mail When Cited PubMed Citation

A rare disease can represent irrelevant esoterica to some but an interesting challenge to others — an oddity or an opportunity. Ogden Bruton's observations in a boy with unusual susceptibility to bacterial infections show how clinical acumen and simple technical means led to the discovery of a new disease, agammaglobulinemia.¹ Echoes of Bruton's case report, which appeared 44 years ago, reverberate in this issue of the Journal with the publication of a paper by Yel et al.² on novel and instructive molecular variants of agammaglobulinemia.

Bruton's patient, a four-year-old boy, was first admitted to Walter Reed Army Hospital because of . . . [Full Text of this Article]

References

HOME  |  SUBSCRIBE  |  SEARCH  |  CURRENT ISSUE  |  PAST ISSUES  |  COLLECTIONS  |  PRIVACY  |  HELP  |  beta.nejm.org Comments and questions? Please contact us. The New England Journal of Medicine is owned, published, and copyrighted © 2008 Massachusetts Medical Society. All rights reserved.