Hurler syndrome, also known as mucopolysaccharidosis type I (MPS I), is a genetic disorder affecting newborns that leads to severe cognitive deficiencies and severe physical abnormalities. Genetic ...

Hurler syndrome, also known as mucopolysaccharidosis ... cognitive deficiencies and severe physical abnormalities. Genetic mutations disrupt synthesis of an essential lysosomal enzyme IDUA ...

Antibiotics that enable ribosomes to "read through" premature stop codons (nonsense mutations), which truncate proteins ... on ribosomes to correct the enzyme deficiency that causes Hurler syndrome, ...

Patients with the disease, called Hurler syndrome, suffer from short stature, spinal defects, and extremely stiff joints, complications that greatly limit their quality of life. But in a new paper ...

Mucopolysaccharidosis type 1, also known as Hurler syndrome, is a rare but life-threatening genetic condition. Babies born with this inherited disorder do not produce an enzyme needed to break down ...

Hurler syndrome, also known as mucopolysaccharidosis ... cognitive deficiencies and severe physical abnormalities. Genetic mutations disrupt synthesis of an essential lysosomal enzyme IDUA ...