Identification of Multiple Sulfatase Deficiency (MSD) in newborn screening: A case study
A patient with multiple sulfatase deficiency (MSD) was identified through a lysosomal storage disorder enzyme analysis panel, based on a characteristic pattern of reduced activities across multiple sulfatases. Newborn screening laboratories implement various quality control protocols to assess the integrity of received samples. The quality control policy for identifying heat-denatured samples evaluates several enzyme activity levels to determine if a sample has been compromised by excessive heat. A new quality control policy has been established to differentiate heat-denatured samples from those affected by Multiple Sulfatase Deficiency.
Authors
- Taraka Donti (ORCID: https://orcid.org/0000-0002-3830-155X)
- James C. DiPerna (ORCID: https://orcid.org/0000-0002-4663-9286)
- Madhuri Hegde (ORCID: https://orcid.org/0000-0002-4500-0368)
Publication Details
- Journal
- Molecular Genetics and Metabolism Reports
- Published
- 2026-01-06
- DOI
- https://doi.org/10.1016/j.ymgmr.2025.101285
- Primary Topic
- Lysosomal Storage Disorders Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00