Literature DB >> 16197847

[Periodic fever: the first Portuguese case-report of hyper-IgD syndrome (HIDS)].

Tiago Tribolet de Abreu1.   

Abstract

BACKGROUND: Periodic fever can have one of multiple causes. Among the hereditary periodic fever syndromes, hyper-IgD syndrome (HIDS) is a possible diagnosis, although, until now, no cases had been described in Portugal. CASE-REPORT: We report a 25-year-old woman, with periodic fever since she was 8 months old. She had high serum IgD levels, and a molecular study of the mevalonate kinase gene was performed. A compound heterozygote was found for two mutations: V377I and T237S. This last mutation had not been observed before. DISCUSSION: We analyse the clinical features that made us think on HIDS as a possible diagnosis, and we highlight the features that are important for the differential diagnosis between HIDS and other periodic fevers.
CONCLUSIONS: HIDS is a possible diagnosis for patients with periodic fever, even in Portugal.

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Year:  2004        PMID: 16197847

Source DB:  PubMed          Journal:  Acta Med Port        ISSN: 0870-399X


  1 in total

1.  Different clinical presentation of the hyperimmunoglobulin D syndrome (HIDS) (four cases from Turkey).

Authors:  Dıdem Arslan Tas; Suzan Dınkcı; Eren Erken
Journal:  Clin Rheumatol       Date:  2012-01-14       Impact factor: 2.980

  1 in total

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