Abstract

There have been significant advances allowing for the integration of mucopolysaccharidosis I into newborn screening programs. Initial experiences using a single-tier approach for this disorder have highlighted shortcomings that require immediate remediation. The recent evaluation of a second-tier biomarker integrated into the MPS I newborn screening protocol has been demonstrated to greatly improve the precision and predictive value of newborn screening for this disorder. This commentary urges newborn screening programs to learn from these experiences and improve newborn screening for mucopolysaccharidosis I and future mucopolysaccharidoses newborn screening programs by implementation of a second-tier biomarker analyte.

Original languageEnglish
Article number91
JournalInternational Journal of Neonatal Screening
Volume6
Issue number4
DOIs
StatePublished - Dec 2020

Keywords

  • Glycosaminoglycans
  • Lysosomal storage disease
  • Mucopolysaccharidoses
  • Pseudodeficiency

Fingerprint

Dive into the research topics of 'Newborn Screening for Mucopolysaccharidosis I: Moving Forward Learning from Experience'. Together they form a unique fingerprint.

Cite this