Hyperimmunoglobulin D Syndrome: Case Report


Sen H., SILAN F., Binnetoglu E., Gunes F., Akurut C., ULUDAĞ A., ...More

ARCHIVES OF RHEUMATOLOGY, vol.30, no.3, pp.244-246, 2015 (Peer-Reviewed Journal) identifier identifier

  • Publication Type: Article / Article
  • Volume: 30 Issue: 3
  • Publication Date: 2015
  • Doi Number: 10.5606/archrheumatol.2015.4986
  • Journal Name: ARCHIVES OF RHEUMATOLOGY
  • Journal Indexes: Science Citation Index Expanded, Scopus, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.244-246
  • Keywords: Hereditary autoinflammatory disease, hyperimmunoglobulin D syndrome, mevalonate kinase mutation, PERIODIC FEVER SYNDROME, HYPER IGD SYNDROME, FOLLOW-UP, ATTACKS, SERIES

Abstract

Hyperimmunoglobulin D syndrome is a rare autosomal recessive inherited disease characterized by fever attacks, which may be accompanied by chills, headache, abdominal pain, and cervical lymphadenopathy. Typical hyperimmunoglobulin D syndrome patients start to show symptoms in the first years of life. Diagnosis is based on the presence of symptoms with reduction in the enzyme activity of mevalonate kinase or by detecting the mutation in the mevalonate kinase gene that causes the disease. In this article, we present a 21-year-old female patient who started having fever attacks in early childhood and was diagnosed with familial Mediterranean fever; however, in spite of treatment, whose complaints did not resolve. The genetic analysis, which detected homozygote mevalonate kinase gene mutation and resulted in the hyperimmunoglobulin D syndrome diagnosis, is presented with an accompanying discussion of the literature.