Late onset GM2 gangliosidosis mimicking spinal muscular atrophy.
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.
Key words
(18)F-FDG PET CT; (18)F-fluorodeoxyglucose positron emission tomography; ALS; FDG-PET; GM2 gangliosidoses; GM2 gangliosidosis type 0; GM2 gangliosidosis type B; GM2-0; GM2-B; GM2G; HEXA gene; Hex A; Hex B; LOGM2; Late onset GM2 ganglisidosis; MLPA; MND; MRI; MRS; MRS (SVS); Motor neuron disease; NAA/Cr; SMA; Spinal muscular atrophy; TE; TSD; TSE; TaySachs disease; amyotrophic lateral sclerosis; fluorodeoxyglucose positron emission tomography; hexosaminidase A; hexosaminidase B; late-onset or chronic GM2 gangliosidoses; mI/Cr; magnetic resonance imaging; magnetic resonance spectroscopy; magnetic resonance spectroscopy single voxel; motor neuron disease; multiplex ligation-dependent probe amplification; myo-inositol/creatine; ratio of the N-acetylaspartate/creatine; spinal muscular atrophy; time echo; time spin echo
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: