Journal of Pediatric Rehabilitation Medicine · 2010 · 17 citations · 18 references
MedicineOrthopaedic SurgeryOrthopedic SurgeryOrthopedicsPediatric OrthopaedicsPediatric Orthopedic SurgeryBone DisordersBone PathologyJoint DisordersLysosomal Storage DisordersMusculoskeletal PathologySpine DisordersLysosomal Storage DefectsMucopolysaccharidosis-associated Skeletal DiseaseMucopolysaccharidosis-associated Skeletal DysplasiaMusculoskeletal DiseaseMusculoskeletal DisordersMusculoskeletal InvolvementOrthopaedic ComplicationsSpine Deformities
Mucopolysaccharidosis (MPS) VI is an inheritable lysosomal storage disorder that is often associated with severe orthopedic problems such as hip dysplasia, spinal deformities, and deformities in the skull, knees and hands. We describe the progression and management of three MPS VI cases with focus on their orthopedic problems.
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Guided Growth for Angular Correction
Peter M. Stevens · Journal of Pediatric Orthopaedics · 2007 · 493 citations
Paul Harmatz, Roberto Giugliani, Ida Vanessa Döederlein Schwartz et al. · The Journal of Pediatrics · 2006 · 364 citations
Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)
Paul Harmatz, Chester B. Whitley, Lewis Waber et al. · The Journal of Pediatrics · 2004 · 274 citations
Paul Harmatz, David Ketteridge, Roberto Giugliani et al. · PEDIATRICS · 2005 · 215 citations