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The British Journal of Radiology, Vol 55, Issue 659 805-812, Copyright © 1982 by British Institute of Radiology
ARTICLES |
DE Paterson, G Harper, HJ Weston and J Mattingley
Mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome) form B is a rare disease occurring in siblings. It may present with radiological features like Perthes' disease or hypothyroidism. We report two such cases, and discuss the differential diagnosis of the spondylo-epiphyseal dysplasias. We stress the importance of final diagnosis by identifying a particular glycosaminoglycan excess in the urine and an enzyme deficiency in the fibroblasts aryl sulphatase B and N-acetylgalactosamine-4-sulphatase.
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