Archives of Pathology & Laboratory Medicine · 2001 · 37 citations · 7 references
Life SciencesGeneticsMolecular GeneticsHuman GeneticsMedical GeneticsMolecular PathologyGenetic DisordersGlycogen MetabolismMolecular AutopsyNeurodegenerative DiseasesNeurodegenerative DisordersGlycogen Storage DiseasesGlycogenesis DisordersGlycosylation In DiseaseMissense MutationsPolyglutamine Diseases
We describe a case of adult polyglucosan body disease with characteristic clinical symptoms of peripheral neuropathy, upper motor neuron signs, and bowel and bladder dysfunction. Sural nerve biopsy revealed diagnostic intra-axonal polyglucosan bodies. On electron microscopic examination, the inclusions were located mainly within myelinated nerve fibers and consisted of branched filaments that were 6 to 8 nm wide. The diagnosis of adult polyglucosan body disease was confirmed by a skin biopsy from the axilla showing similar inclusions in myoepithelial cells of apocrine glands. This report provides additional evidence that skin biopsy, to date advocated by a single case report only, may be a less invasive and simpler diagnostic alternative to sural nerve or brain biopsies.
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