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Published in: Journal of Inherited Metabolic Disease 2/2013

Open Access 01-03-2013 | Original Article

Spinal involvement in mucopolysaccharidosis IVA (Morquio-Brailsford or Morquio A syndrome): presentation, diagnosis and management

Authors: Guirish A. Solanki, Kenneth W. Martin, Mary C. Theroux, Christina Lampe, Klane K. White, Renée Shediac, Christian G. Lampe, Michael Beck, William G. Mackenzie, Christian J. Hendriksz, Paul R. Harmatz

Published in: Journal of Inherited Metabolic Disease | Issue 2/2013

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Abstract

Mucopolysaccharidosis IVA (MPS IVA), also known as Morquio-Brailsford or Morquio A syndrome, is a lysosomal storage disorder caused by a deficiency of the enzyme N-acetyl-galactosamine-6-sulphate sulphatase (GALNS). MPS IVA is multisystemic but manifests primarily as a progressive skeletal dysplasia. Spinal involvement is a major cause of morbidity and mortality in MPS IVA. Early diagnosis and timely treatment of problems involving the spine are critical in preventing or arresting neurological deterioration and loss of function. This review details the spinal manifestations of MPS IVA and describes the tools used to diagnose and monitor spinal involvement. The relative utility of radiography, computed tomography (CT) and magnetic resonance imaging (MRI) for the evaluation of cervical spine instability, stenosis, and cord compression is discussed. Surgical interventions, anaesthetic considerations, and the use of neurophysiological monitoring during procedures performed under general anaesthesia are reviewed. Recommendations for regular radiological imaging and neurologic assessments are presented, and the need for a more standardized approach for evaluating and managing spinal involvement in MPS IVA is addressed.
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Metadata
Title
Spinal involvement in mucopolysaccharidosis IVA (Morquio-Brailsford or Morquio A syndrome): presentation, diagnosis and management
Authors
Guirish A. Solanki
Kenneth W. Martin
Mary C. Theroux
Christina Lampe
Klane K. White
Renée Shediac
Christian G. Lampe
Michael Beck
William G. Mackenzie
Christian J. Hendriksz
Paul R. Harmatz
Publication date
01-03-2013
Publisher
Springer Netherlands
Published in
Journal of Inherited Metabolic Disease / Issue 2/2013
Print ISSN: 0141-8955
Electronic ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-013-9586-2

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