Tricuspid endocarditis in hyper-IgE syndrome

Hyper-IgE syndrome is a congenitally acquired primary immune deficiency condition. We report a case of possible hyper-IgE syndrome who presented with multiple cold skin abscesses and chest infection due to <i>Staphylococcus aureus </i>and hyper-IgE findings. Patient also had tricuspid va...

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Bibliographic Details
Main Authors: Gupta S, Mittal A, Jagdish
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2010-01-01
Series:Journal of Postgraduate Medicine
Subjects:
Online Access:http://www.jpgmonline.com/article.asp?issn=0022-3859;year=2010;volume=56;issue=2;spage=143;epage=145;aulast=Gupta