Mevalonate kinase deficiency (MKD) is an autosomal recessive metabolic disorder
associated with recurrent autoinflammatory episodes. The disorder is caused by bi-allelic …

Mevalonate kinase deficiency (MKD) is an autosomal recessive autoinflammatory disorder
caused by mutations in the MVK gene resulting in deficient activity of mevalonate kinase …

Mevalonate kinase deficiency (MKD) is an autoinflammatory metabolic disorder caused by
bi‐allelic loss‐of‐function variants in the MVK gene, resulting in decreased activity of the …

Mevalonate kinase deficiency (MKD) is characterized by recurrent fevers and flares of
systemic inflammation, caused by biallelic loss-of-function mutations in MVK. The underlying …

Mevalonate kinase deficiency (MKD) is an autoinflammatory disorder caused by mutations
in the MVK gene resulting in decreased activity of the enzyme mevalonate kinase (MK) …

The rare autoinflammatory disease mevalonate kinase deficiency (MKD, which includes
HIDS and mevalonic aciduria) is caused by recessive, pathogenic variants in the MVK gene …

Mevalonate kinase deficiency (MKD) is an autosomal recessive auto‑inflammatory disease,
caused by impairment of the mevalonate pathway. Although the molecular mechanism …

Mevalonate kinase (MK)-associated diseases encompass a broad spectrum of rare auto-
inflammatory conditions, all resulting from pathogenic variants in the mevalonate kinase …

Mevalonate kinase deficiency (MKD) is a recessively inherited autoinflammatory disorder
with a spectrum of manifestations, including the well-defined clinical phenotypes of …

Hyper-IgD and periodic fever syndrome (HIDS) and mevalonic aciduria are autosomal
recessive disorders characterized by recurrent episodes of fever and generalized …