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HIDS/MKD

Hyperimmunoglobulin D Syndrome / Mevalonate kinase deficiency

Hyperimmunoglobulin D Syndrome is a genetic syndrome accompanied by recurrent bouts of fever. Usually the hyperimmunoglobulin D Syndrome already begins in the first year of life. Most of the attacks are accompanied by swellings of the cervical lymph nodes, abdominal pain and vomiting, diarrhoea or both. Headaches, joint pain or inflammation of the large joints and rashes develop frequently.

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