Article ID Journal Published Year Pages File Type
1998724 Molecular Genetics and Metabolism 2013 5 Pages PDF
Abstract

A 12 year-old female presented with a seven-year history of progressive muscle weakness, atrophy, tremor and fasciculations. Cognition was normal. Rectal biopsy revealed intracellular storage material and biochemical testing indicated low hexosaminidase activity consistent with juvenile-onset GM2-gangliosidosis. Genetic evaluation revealed compound heterozygosity with two novel mutations in the hexosaminidase β-subunit (c.512-3 C>A and c.1613+15_1613+18dup). Protein analysis was consistent with biochemical findings and indicated only a small portion of β-subunits were properly processed. These results provide additional insight into juvenile-onset GM2-gangliosidoses and further expand the number of β-hexosaminidase mutations associated with motor neuron disease.

► Child presented with Sandhoff disease chemically similar of “Hexosaminidase Paris”. ► Rectal biopsy revealed storage material in cells between the mucosa and submucosa. ► Evaluation revealed two mutations causing a cryptic splice site and exon skipping. ► Most of the mutant protein was misfolded and retained in the endoplasmic reticulum. ► Miglustat treatment was ineffective, initiation may have been too late for response.

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