Literature DB >> 15205860

Brain MRI findings in patients with mucopolysaccharidosis types I and II and mild clinical presentation.

M Gisele Matheus1, Mauricio Castillo, J Keith Smith, Diane Armao, Diane Towle, Joseph Muenzer.   

Abstract

Our objective was to determine the brain magnetic resonance imaging (MRI) abnormalities in a selected group of patients with mucopolysaccharidosis (MPS) types I and II who had only mild clinical manifestations. We retrospectively assessed MRI brain studies in 18 patients with MPS (type I: 6 and type II: 12). We evaluated abnormal signal intensity in the white matter, widening of the cortical sulci, size of the supratentorial ventricles, dilatation of the perivascular spaces (PVS) and enlargement of the subarachnoid spaces. We observed a broad spectrum of findings, and despite severely abnormal MRI studies, no patients had mental retardation. We also observed that dilated PVS, previously believed to be caused by macroscopic deposition of the mucopolysaccharides, had an appearance similar to cerebrospinal fluid (CSF) in all MRI sequences performed, even in FLAIR and trace diffusion weighted images. Based on our results, we believe that with the exception of white matter abnormalities and brain atrophy, all other findings may be related to abnormal resorption of CSF, and there is no relationship between the imaging and clinical manifestations of the disease.

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Year:  2004        PMID: 15205860     DOI: 10.1007/s00234-004-1215-1

Source DB:  PubMed          Journal:  Neuroradiology        ISSN: 0028-3940            Impact factor:   2.804


  21 in total

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Journal:  Neuroradiology       Date:  1977-12-31       Impact factor: 2.804

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Journal:  Neuroradiology       Date:  1990       Impact factor: 2.804

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Journal:  Neuroradiology       Date:  1996-07       Impact factor: 2.804

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Journal:  Curr Neurol Neurosci Rep       Date:  2005-03       Impact factor: 5.081

Review 7.  Mucopolysaccharidoses: overview of neuroimaging manifestations.

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Journal:  Pediatr Radiol       Date:  2018-05-11

8.  A Clinically Severe Variant of β-Mannosidosis, Presenting with Neonatal Onset Epilepsy with Subsequent Evolution of Hydrocephalus.

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9.  Features of brain MRI in dogs with treated and untreated mucopolysaccharidosis type I.

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Journal:  PLoS One       Date:  2009-02-10       Impact factor: 3.240

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