[Hyper-IgD-syndrome].

Abstract:

UNLABELLED:We report on a 6-year-old Romanian girl with recently diagnosed hyper-IgD-syndrome. The leading symptom of this rare disease are periodic pyrexia, joint involvements (arthralgias/arthritis) and swollen lymph nodes. A permanent increase of alpha 1-acid glycoprotein fucosylation indicates persisting inflammation. Most important in differential diagnosis in familial Mediterranean fever. Therapy is merely supportive as yet, the long-term outlook seems good despite duration of the illness. CONCLUSION:the hyper-IgD-syndrome must be considered in cases of otherwise unexplained periodic fever.

journal_name

Z Rheumatol

authors

Suschke J,Walther JU

doi

10.1007/s003930050019

subject

Has Abstract

pub_date

1997-01-01 00:00:00

pages

40-2

issue

1

eissn

0340-1855

issn

1435-1250

journal_volume

56

pub_type

杂志文章
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  • [Rheumatism and art : Max Slevogt. The bon viveur and artist plagued by gout].

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