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

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
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article

Identification of Multiple Sulfatase Deficiency (MSD) in newborn screening: A case study

Taraka Donti, James C. DiPerna, Madhuri Hegde
Molecular Genetics and Metabolism Reports
Lysosomal Storage Disorders Research
article

Identification of Multiple Sulfatase Deficiency (MSD) in newborn screening: A case study

Taraka Donti, James C. DiPerna, Madhuri Hegde
article en

Abstract

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.

Molecular Genetics and Metabolism ReportsVol. 46
Openalex Percentile: Top 96%
Lysosomal Storage Disorders Research
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