Immunochemistry of lysosomal storage disorders

Emma Parkinson-Lawrence, Maria Fuller, John J. Hopwood, Peter J. Meikle, Doug A. Brooks

Research output: Contribution to journalReview articlepeer-review

22 Citations (Scopus)

Abstract

Background: Lysosomal storage disorders are a group of genetic diseases, each with a broad spectrum of clinical presentation that ranges from attenuated to severe. The immunochemical analysis of patient samples is aimed at several key aspects of patient management, including early detection of the disorder, prediction of clinical severity, determining the most appropriate therapeutic regimen, and monitoring of patients on therapy. Methods: In this study, we review the current and emerging technology available to achieve these assessments. Results: Immune assays have direct practical application for the early detection, diagnosis and prognosis of lysosomal storage disorder patients. Multiplexing of these assays may provide a platform to allow newborn screening for multiple lysosomal storage disorders. Conclusions: We have reviewed the immunochemical techniques available for the analysis of lysosomal storage disorder patient samples and advise that these may be used in conjunction with other technologies for effective patient management.

Original languageEnglish
Pages (from-to)1660-1668
Number of pages9
JournalClinical chemistry
Volume52
Issue number9
DOIs
Publication statusPublished or Issued - Sep 2006

ASJC Scopus subject areas

  • Clinical Biochemistry
  • Biochemistry, medical

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