Add to ORKG"Hunter Syndrome (HS) is a multisystemic disorder characterized by glycosaminoglycan (GAG) accumulation due to enzyme deficiency of iduronate 2-sulfatase. This case report characterizes visual pathway involvement in HS.
Abstract Hunter syndrome (mucopolysaccharidosis II [MPS II]) is characterized by lysosomal glycosami...
Hunter's disease is a mucopolysaccharidosis inherited in an X-linked recessive pattern. Optic disc s...
This review aims to provide clinicians in Latin America with the most current information on the cli...
Hunter syndrome is a Type II mucopolysaccharidoses (MPS) metabolic disorder that is defined by a def...
Hunters disease is a rare genetic disorder caused by the abnormal buildup of compounds called glycoa...
Hunter syndrome is a rare, X-linked disorder caused by a deficiency of the lysosomal enzyme iduronat...
Hunter syndrome is a rare X-linked recessive disorder caused by deficiency of the lysosomal enzyme i...
Background. This clinical case of orphan disease can be interesting for its early diagnostics which ...
This review aims to provide clinicians in Latin America with the most current information on the cli...
Hunter syndrome or mucopolysaccharidosis (MPS) type II is an X-linked recessive disorder caused by a...
Hunter's Syndrome or mucopolysaccharidosis Type II is a rare metabolic disorder caused by the defici...
Hunter syndrome is a lysosomal disease characterized by deficiency of the lysosomal enzyme iduronate...
The mucopolysaccharidoses are a group of inherited disorders of lysosomal storage of glycosaminoglyc...
Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is a rare X-linked lysosomal storage disease...
Hunter syndrome (or Mucopolysaccharidosis type II, MPS II) is an X-linked recessive disorder due to ...
Abstract Hunter syndrome (mucopolysaccharidosis II [MPS II]) is characterized by lysosomal glycosami...
Hunter's disease is a mucopolysaccharidosis inherited in an X-linked recessive pattern. Optic disc s...
This review aims to provide clinicians in Latin America with the most current information on the cli...
Hunter syndrome is a Type II mucopolysaccharidoses (MPS) metabolic disorder that is defined by a def...
Hunters disease is a rare genetic disorder caused by the abnormal buildup of compounds called glycoa...
Hunter syndrome is a rare, X-linked disorder caused by a deficiency of the lysosomal enzyme iduronat...
Hunter syndrome is a rare X-linked recessive disorder caused by deficiency of the lysosomal enzyme i...
Background. This clinical case of orphan disease can be interesting for its early diagnostics which ...
This review aims to provide clinicians in Latin America with the most current information on the cli...
Hunter syndrome or mucopolysaccharidosis (MPS) type II is an X-linked recessive disorder caused by a...
Hunter's Syndrome or mucopolysaccharidosis Type II is a rare metabolic disorder caused by the defici...
Hunter syndrome is a lysosomal disease characterized by deficiency of the lysosomal enzyme iduronate...
The mucopolysaccharidoses are a group of inherited disorders of lysosomal storage of glycosaminoglyc...
Mucopolysaccharidosis type II (MPS II, Hunter syndrome) is a rare X-linked lysosomal storage disease...
Hunter syndrome (or Mucopolysaccharidosis type II, MPS II) is an X-linked recessive disorder due to ...
Abstract Hunter syndrome (mucopolysaccharidosis II [MPS II]) is characterized by lysosomal glycosami...
Hunter's disease is a mucopolysaccharidosis inherited in an X-linked recessive pattern. Optic disc s...
This review aims to provide clinicians in Latin America with the most current information on the cli...