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Late onset GM2 gangliosidosis mimicking spinal muscular atrophy.
Jamrozik, Z; Lugowska, A; Golebiowski, M; Królicki, L; Maczewska, J; Kuzma-Kozakiewicz, M.
Affiliation
  • Jamrozik Z; Department of Neurology, Medical University of Warsaw, Poland. zygmunt.jamrozik@wum.edu.pl
Gene ; 527(2): 679-82, 2013 Sep 25.
Article in En | MEDLINE | ID: mdl-23820084
A case of late onset GM2 gangliosidodis with spinal muscular atrophy phenotype followed by cerebellar and extrapyramidal symptoms is presented. Genetic analysis revealed compound heterozygous mutation in exon 10 of the HEXA gene. Patient has normal intelligence and emotional reactivity. Neuroimaging tests of the brain showed only cerebellar atrophy consistent with MR spectroscopy (MRS) abnormalities. (18)F-fluorodeoxyglucose positron emission tomography (18)F-FDG PET/CT of the brain revealed glucose hypometabolism in cerebellum and in temporal and occipital lobes bilaterally.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscular Atrophy, Spinal / Gangliosidoses, GM2 Type of study: Diagnostic_studies Limits: Adult / Humans / Male Language: En Journal: Gene Year: 2013 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscular Atrophy, Spinal / Gangliosidoses, GM2 Type of study: Diagnostic_studies Limits: Adult / Humans / Male Language: En Journal: Gene Year: 2013 Document type: Article Affiliation country: Country of publication: