- Hyper IgD syndrome
- Hyperimmunoglobinemia D with recurrent fever
- Hyperimmunoglobulinemia D and periodic fever syndrome
- Hyperimmunoglobulinemia D syndrome
There is no cure for hyper IgD syndrome and currently no established treatment. Management is focused on supportive care. Some patients have responded to high-dose prednisone. Simvastatin, Anakinria (an IL-1 receptor antagonist) and TNF inhibitors have recently shown some success in controlling inflammatory attacks.
Consultations with the following specialists may be helpful: dermatologist, rheumatologist, and infectious disease specialist (to evaluate periodic fever).
- Shinawi M, Scaglia F. Hereditary Periodic Fever Syndromes. Medscape Reference. 2013; http://emedicine.medscape.com/article/952254-overview. Accessed 3/5/2013.
- Frenkel J, Simon A. Hyperimmunoglobulinemia D with recurrent fever. Orphanet. 2011; http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=343. Accessed 3/5/2013.
- ClinicalTrials.gov lists trials that are studying or have studied Hyper-IgD syndrome. Click on the link to go to ClinicalTrials.gov to read descriptions of these studies.