BackgroundMucopolysaccharidosis type I (MPS-I) is a lysosomal storage disorder characterized by progressive multi-organ disease. The standard of care for patients with the severe phenotype (Hurler syndrome, MPS I-H) is early hematopoietic stem cell transplantation (HSCT). However, skeletal disease, including hip dysplasia, is almost invariably present in MPS I-H, and appears to be particularly unresponsive to HSCT. Hip dysplasia may lead to pain and loss of ambulation, at least in a subset of patients, if left untreated. However, there is a lack of evidence to guide the development of clinical guidelines for the follow-up and treatment of hip dysplasia in patients with MPS I-H. Therefore, an international Delphi consensus procedure was init...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
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...
BackgroundMucopolysaccharidosis type I (MPS-I) is a lysosomal storage disorder characterized by prog...
The introduction of hematopoietic stem cell transplantation (HSCT) has significantly improved the li...
Background: Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder that results in th...
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder that results in the accumulatio...
Mucopolysaccharidosis type I (MPS I; Hurler syndrome) is a lysosomal storage disease caused by a def...
The introduction of hematopoietic stem cell transplantation (HSCT) has significantly improved the li...
Abstract Mucopolysaccharidosis I-Hurler (MPS I-H) is the most severe form of a metabolic genetic dis...
Background: In all patients with mucopolysaccharidosis type I (MPS I), skeletal disease (dysostosis ...
Introduction. Morquio syndrome or mucopolysaccharidosis (MPS) type IV is a rare autosomal recessive ...
Abstract Background In all patients with mucopolysaccharidosis type I (MPS I), skeletal disease (dys...
Children affected by mucopolysaccharidosis (MPS) type IH (Hurler Syndrome), an autosomal recessive m...
The mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders with clinical m...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
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...
BackgroundMucopolysaccharidosis type I (MPS-I) is a lysosomal storage disorder characterized by prog...
The introduction of hematopoietic stem cell transplantation (HSCT) has significantly improved the li...
Background: Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder that results in th...
Mucopolysaccharidosis type I (MPS I) is a lysosomal storage disorder that results in the accumulatio...
Mucopolysaccharidosis type I (MPS I; Hurler syndrome) is a lysosomal storage disease caused by a def...
The introduction of hematopoietic stem cell transplantation (HSCT) has significantly improved the li...
Abstract Mucopolysaccharidosis I-Hurler (MPS I-H) is the most severe form of a metabolic genetic dis...
Background: In all patients with mucopolysaccharidosis type I (MPS I), skeletal disease (dysostosis ...
Introduction. Morquio syndrome or mucopolysaccharidosis (MPS) type IV is a rare autosomal recessive ...
Abstract Background In all patients with mucopolysaccharidosis type I (MPS I), skeletal disease (dys...
Children affected by mucopolysaccharidosis (MPS) type IH (Hurler Syndrome), an autosomal recessive m...
The mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders with clinical m...
Mucopolysaccharidosis type I-Hurler syndrome (MPS-IH) is a lysosomal storage disease characterized b...
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...