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Mevalonic aciduria

MONDO:0012481

Mevalonic aciduria (MVA) is a rare, very severe form of mevalonate kinase deficiency (MKD) characterized by dysmorphic features, failure to thrive, psychomotor delay, ocular involvement, hypotonia, progressive ataxia, myopathy, and recurrent inflammatory episodes.

Also known as: HIDS, MKD, MVA, complete mevalonate kinase deficiency, hyperimmunoglobulin D with periodic fever syndrome, mevalonic aciduria, MEVA, Mevalonicaciduria

11 clinical trials for this condition and its sub-types, 0 tagged with Mevalonic aciduria itself.

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