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- W2982346376 abstract "Mevalonate kinase deficiency (MKD) is a rare autosomal recessive autoinflammatory disease caused by mutations in the mevalonate kinase (MVK) gene. It is characterized by recurrent attacks of fever mostly associated with cervical lymphadenopathy, cutaneous, digestive, and musculoskeletal manifestations. Disease activity may decrease with time or remain high. Anti-interleukin-1 agents are often effective in controlling and preventing flares in patients with severe forms of MKD." @default.
- W2982346376 created "2019-11-08" @default.
- W2982346376 creator A5046909004 @default.
- W2982346376 date "2019-10-30" @default.
- W2982346376 modified "2023-10-18" @default.
- W2982346376 title "Mevalonate Kinase Deficiency" @default.
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- W2982346376 doi "https://doi.org/10.1007/978-3-030-19055-2_12" @default.
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