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ECR 2019 / C-1613
Mucopolysaccharidoses: brain and spinal MRI findings.
Congress: ECR 2019
Poster No.: C-1613
Type: Educational Exhibit
Keywords: Metabolic disorders, Diagnostic procedure, MR, Paediatric, Neuroradiology spine
Authors: A. Navarro Baño1, C. Fernández Hernández1, C. Serrano Garcia1, R. M. Sánchez Jiménez1, J. M. Felices Farias1, F. Barqueros Escuer1, D. Páez Granda1, I. Sánchez Serrano2, I. Vicente Zapata2; 1El Palmar, Murcia/ES, 2Murcia/ES


Mucopolysaccharidoses are chronic diseases of lysosomal deposit, progressive and multisystemic, caused by deficiency of enzymes that degrade mucopolysaccharides, which causes a deposit in multiple tissues, including brain tissue, as well as causes alterations in the spine.

Through a review of cases of children with MPS from our hospital, typical images are described, mainly from the MPS type I (Hurler).


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