Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Syndromic disease · Lysosomal storage disease with skeletal involvement · Mucopolysaccharidosis type 1
Hurler syndrome
Hurler syndrome is the most severe form of mucopolysaccharidosis type 1 (MPS1), a rare lysosomal storage disease, characterized by skeletal abnormalities, cognitive impairment, heart disease, respiratory problems, enlarged liver and spleen, characteristic facies and reduced life expectancy.
This condition has no sub-types.