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...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2010-01-01
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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 |