The US Secretary of Health and Human Services recommended in February 2016 that mucopolysaccharidosis type 1 (MPS I) be added to the recommended uniform screening panel for state newborn screening programs. One of the key factors in this decision was the evidence suggesting that earlier treatment with hematopoietic cell transplantation (HCT) for the most severe form, Hurler syndrome (MPS IH), would lead to improved cognitive outcomes. Consistent evidence from peer-reviewed studies suggests that transplantation in the first year of life is associated with improved developmental quotient or intelligence quotient and continued cognitive growth, with earlier age of treatment associated with improved outcomes. However, available evidence suggest...
Mucopolysaccharidosis type II (MPS II - Hunter syndrome) is an X-linked lysosomal storage disorder c...
Mucopolysaccharidosis type I (MPS I; Hurler syndrome) is a lysosomal storage disease caused by a def...
ObjectivesTo characterize the clinical course of mucopolysaccharidosis type IIIA (MPS IIIA), and ide...
Mucopolysaccharidosis type I (MPS I) was added to the Recommended Uniform Screening Panel for newbor...
Abstract Background Newborn screening for mucopolysaccharidosis type I (MPS I) shows promise to impr...
Purpose: Early treatment is critical for mucopolysaccharidosis type I (MPS I), justifying its incorp...
Objectives: Precise characterization of cognitive outcomes and factors that contribute to cognitive ...
Abstract Background Hurler syndrome (MPS IH), the severe, neurodegenerative form of type one mucopol...
Mucopolysaccharidosis I-Hurler (MPS I-H) is the most severe form of a metabolic genetic disease caus...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
Abstract Mucopolysaccharidosis I-Hurler (MPS I-H) is the most severe form of a metabolic genetic dis...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is an X-linked condition caus...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
In this study, we aimed to describe the natural history of mucopolysaccharidosis I
Mucopolysaccharidosis type II (MPS II - Hunter syndrome) is an X-linked lysosomal storage disorder c...
Mucopolysaccharidosis type I (MPS I; Hurler syndrome) is a lysosomal storage disease caused by a def...
ObjectivesTo characterize the clinical course of mucopolysaccharidosis type IIIA (MPS IIIA), and ide...
Mucopolysaccharidosis type I (MPS I) was added to the Recommended Uniform Screening Panel for newbor...
Abstract Background Newborn screening for mucopolysaccharidosis type I (MPS I) shows promise to impr...
Purpose: Early treatment is critical for mucopolysaccharidosis type I (MPS I), justifying its incorp...
Objectives: Precise characterization of cognitive outcomes and factors that contribute to cognitive ...
Abstract Background Hurler syndrome (MPS IH), the severe, neurodegenerative form of type one mucopol...
Mucopolysaccharidosis I-Hurler (MPS I-H) is the most severe form of a metabolic genetic disease caus...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
Abstract Mucopolysaccharidosis I-Hurler (MPS I-H) is the most severe form of a metabolic genetic dis...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is an X-linked condition caus...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
In this study, we aimed to describe the natural history of mucopolysaccharidosis I
Mucopolysaccharidosis type II (MPS II - Hunter syndrome) is an X-linked lysosomal storage disorder c...
Mucopolysaccharidosis type I (MPS I; Hurler syndrome) is a lysosomal storage disease caused by a def...
ObjectivesTo characterize the clinical course of mucopolysaccharidosis type IIIA (MPS IIIA), and ide...