Skeletal complications in mucopolysaccharidosis VI patients: Case reports

Paula Garcia, Sérgio B. Sousa, Tah Pu Ling, Mário José da Conceição, J. Seabra, Klane K. White, Luísa Diogo

Journal of Pediatric Rehabilitation Medicine · 2010 · 17 citations · 18 references

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Abstract

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.

References

18