Molecular Genetics and Metabolism Reports (Jan 2014)

Development of a fluorometric microtiter plate based enzyme assay for MPS IVA (Morquio type A) using dried blood spots

  • Anirudh J. Ullal,
  • David S. Millington,
  • Deeksha S. Bali

DOI
https://doi.org/10.1016/j.ymgmr.2014.10.004
Journal volume & issue
Vol. 1, no. C
pp. 461 – 464

Abstract

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Mucopolysaccharidosis type IVA or Morquio type-A disease is a hereditary lysosomal storage disorder caused by deficient activity of the lysosomal enzyme N-acetylgalactosamine-6-sulfate sulfatase (GALNS). The disease is caused by lysosomal accumulation of unprocessed glycosaminoglycans (GAGs) that manifests with severe to mild skeletal and cardiopulmonary abnormalities. We have developed a modified microtiter plate-based enzyme activity assay using dried blood spots and a fluorescent substrate for measuring specific GALNS activity to identify patients with MPS IVA.

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