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Title: [Periodic fever: the first Portuguese case-report of hyper-IgD syndrome (HIDS)]. Author: Abreu TT. Journal: Acta Med Port; 2004; 17(5):391-4. PubMed ID: 16197847. 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.[Abstract] [Full Text] [Related] [New Search]