Mevalonic aciduria

Disease Export to PDF
Name:
Mevalonic aciduria
Description:
A rare, 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.
ORPHAcode:
29
Synonyms:
Complete mevalonate kinase deficiency
MVA
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14