Abstract Mucopolysaccharidoses (MPS) are a group of diseases characterized by abnormal accumulation of glycosaminoglycans (GAGs). Although there are differences among the various disease types, the osteoarticular system is always involved. The aim of the present study was to establish a framework for MPS-related orthopaedic manifestations and for their treatment. The authors, affiliated to three different Italian Orthopaedic Centres, report data taken from the literature reviewed in light of their accumulated professional experience. Bone alterations make up what is known as dysostosis multiplex, involving the trunk and limbs and with typical radiological findings. Joints are affected by pathological tissue infiltrations. The cervical spina...
The mucopolysaccharidoses (MPSs) are a group of rare genetic disorders of glycosaminoglycan cataboli...
Mucopolysaccharidosis IVA (MPS IVA), also known as Morquio-Brailsford or Morquio A syndrome, is a ly...
Mucopolysaccharidosis (MPS) and Mucolipidosis (ML II and III) are lysosomal storage disorders with m...
Skeletal abnormalities are an early and prominent feature of most mucopolysaccharide (MPS) disorders...
The mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders with clinical m...
Introduction The accumulation of glycosaminoglycan (GAGs) in the tissues in Mucopolysaccharidoses (M...
Abstract. With advances in the treatment of the mucopolysaccharidosis (MPS) disorders, musculoskelet...
The hips are frequently involved in inheritable diseases which affect the bones. The clinical and ra...
The hips are frequently involved in inheritable diseases which affect the bones. The clinical and ra...
Introduction. Morquio syndrome or mucopolysaccharidosis (MPS) type IV is a rare autosomal recessive ...
Mucopolysaccharidoses (MPS) represent a group of inheritable lysosomal storage diseases caused by mu...
Mucopolysaccharidoses (MPS) represent a group of inheritable lysosomal storage diseases caused by mu...
Abstract: Patients with mucopolysaccharidosis type IVA (MPS IVA; Morquio A syndrome) have accumulati...
Mucopolysaccharidosis (MPS) is a group of disorders caused by the reduced or absent activity of enzy...
Mucopolysaccharidosis IVA (MPS IVA), also known as Morquio-Brailsford or Morquio A syndrome, is a ly...
The mucopolysaccharidoses (MPSs) are a group of rare genetic disorders of glycosaminoglycan cataboli...
Mucopolysaccharidosis IVA (MPS IVA), also known as Morquio-Brailsford or Morquio A syndrome, is a ly...
Mucopolysaccharidosis (MPS) and Mucolipidosis (ML II and III) are lysosomal storage disorders with m...
Skeletal abnormalities are an early and prominent feature of most mucopolysaccharide (MPS) disorders...
The mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders with clinical m...
Introduction The accumulation of glycosaminoglycan (GAGs) in the tissues in Mucopolysaccharidoses (M...
Abstract. With advances in the treatment of the mucopolysaccharidosis (MPS) disorders, musculoskelet...
The hips are frequently involved in inheritable diseases which affect the bones. The clinical and ra...
The hips are frequently involved in inheritable diseases which affect the bones. The clinical and ra...
Introduction. Morquio syndrome or mucopolysaccharidosis (MPS) type IV is a rare autosomal recessive ...
Mucopolysaccharidoses (MPS) represent a group of inheritable lysosomal storage diseases caused by mu...
Mucopolysaccharidoses (MPS) represent a group of inheritable lysosomal storage diseases caused by mu...
Abstract: Patients with mucopolysaccharidosis type IVA (MPS IVA; Morquio A syndrome) have accumulati...
Mucopolysaccharidosis (MPS) is a group of disorders caused by the reduced or absent activity of enzy...
Mucopolysaccharidosis IVA (MPS IVA), also known as Morquio-Brailsford or Morquio A syndrome, is a ly...
The mucopolysaccharidoses (MPSs) are a group of rare genetic disorders of glycosaminoglycan cataboli...
Mucopolysaccharidosis IVA (MPS IVA), also known as Morquio-Brailsford or Morquio A syndrome, is a ly...
Mucopolysaccharidosis (MPS) and Mucolipidosis (ML II and III) are lysosomal storage disorders with m...