Abstract
We report a 73-year-old patient with acid maltase deficiency who initially had been suspected of having motor neuron disease. We discuss clinical and electrophysiological features of muscular lysosomal glycogenosis, with special emphasis on the histopathological differential diagnosis of the disease.
Publication types
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Case Reports
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English Abstract
MeSH terms
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Aged
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Biopsy
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Diagnosis, Differential
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Electromyography
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Female
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Glucan 1,4-alpha-Glucosidase / deficiency
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Glycogen Storage Disease Type II / diagnosis*
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Glycogen Storage Disease Type II / pathology
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Humans
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Muscle Weakness / diagnosis
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Muscle Weakness / pathology
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Muscle, Skeletal / pathology
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Muscular Atrophy / diagnosis
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Muscular Atrophy / pathology
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Neurologic Examination
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Neuromuscular Diseases / diagnosis*
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Neuromuscular Diseases / pathology
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Paralysis / diagnosis
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Paralysis / pathology
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alpha-Glucosidases
Substances
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alpha-Glucosidases
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Glucan 1,4-alpha-Glucosidase