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Articular Syndrome Characteristics in Children with Mucopolysaccharidosis Type I

Background. Mucopolysaccharidosis type I is disease from the group of lysosomal storage disease developing due to mutations in the IDUA gene. It leads to the accumulation of glycosaminoglycans (GAGs) in organs and tissues. Joints damage in this disease is systemic and progressive.Objective. The aim...

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Main Authors: Nato D. Vashakmadze (Author), Mikhail M. Kostik (Author), Nataliya V. Zhurkova (Author), Nataliya V. Buchinskaia (Author), Ekaterina Yu. Zakharova (Author), Margarita A. Soloshenko (Author)
Format: Book
Published: "Paediatrician" Publishers LLC, 2021-12-01T00:00:00Z.
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