Article

Prevalence rates of mucopolysaccharidosis in Iraq: a retrospective cross-sectional observational study

2023-04-13

Abstract excerpt

<h4>Background: </h4> Mucopolysaccharidosis (MPS) is a rare hereditary inborn error of metabolism that represents the largest heterogeneous group of lysosomal storage diseases (LSD) and is characterized by multiorgan impairment due to glycosaminoglycans (GAGs) accumulation in various tissues and organs, resulting in severe frailty and early death. This research aimed to figure out the specific and overall birth pr...

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Literature Corpus work: d6e466b3-1cdf-553a-8c91-3351819bc1a8
DOI: 10.12688/f1000research.130672.1

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