Hip pathologies in mucopolysaccharidosis type III
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DOI: 10.1186/s13018-021-02340-6
Abstract: Background Mucopolysaccharidosis type III (MPS III) comprises a group of rare lysosomal storage diseases. Although musculoskeletal symptoms are less pronounced than in other MPS subtypes, pathologies of hip and spine have been reported in MPS… read more here.
Keywords: mucopolysaccharidosis type; iii patients; hip; hip pathologies ... See more keywords
Sanfilippo Syndrome: Optimizing Care with a Multidisciplinary Approach
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DOI: 10.2147/jmdh.s362994
Abstract: Abstract Sanfilippo syndrome, or mucopolysaccharidosis type III (MPS III), is a disease grouping five genetic disorders, four of them occurring in humans and one known to date only in a mouse model. In every subtype… read more here.
Keywords: multidisciplinary approach; optimizing care; care multidisciplinary; mps iii ... See more keywords
Neurological, neurobehavioral, and radiological alterations in patients with mucopolysaccharidosis III (Sanfilippo's syndrome) in Brazil
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DOI: 10.3389/fneur.2022.968297
Abstract: Mucopolysaccharidosis type III (MPS III) or Sanfilippo syndrome is the most common form of MPS, in which neurological involvement in all stages of the disease is prominent. The current study aimed to comprehensively describe the… read more here.
Keywords: iii sanfilippo; neurological neurobehavioral; age; neurobehavioral radiological ... See more keywords
Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III
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DOI: 10.3390/jpm12050665
Abstract: Background: Mucopolysaccharidosis type III (MPS III) is an autosomal recessive lysosomal storage disorder characterised by progressive neurocognitive deterioration. MPS III subtypes are clinically indistinguishable, with a wide range of symptoms and variable severity. The natural… read more here.
Keywords: natural history; mucopolysaccharidosis type; type iii; retardation ... See more keywords