Adult Onset Familial Cherry-Red Spot Myoclonus

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Adult Onset Familial Cherry-Red Spot Myoclonus

We report a case of a 36-year-old woman with progressive generalized myoclonus that first became apparent 9 years ago. Her younger brother had similar problems. Examination of her eyes revealed cherry-red spots. Hexosaminidase A, β-galactosidase and neuraminidase activity were normal. Although the laboratory findings were negative, cherry-red spots, progressive myoclonus and autosomal recessive...

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Cherry-red spot myoclonus syndrome and alpha-neuraminidase deficiency: neurophysiological, pharmacological and biochemical study in an adult.

A 22 year old patient with non-familial progressive myoclonus, macular cherry-red spot, moderate cerebellar syndrome and normal intelligence is described. The myoclonus began at the age of 18 years. Focal myoclonus could easily be elicited by voluntary and passive movements, and by touch and electrical stimulation of median nerve. Somatosensory evoked potentials showed a high voltage early comp...

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Adult-onset opsoclonus-myoclonus syndrome.

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Typical ophthalmoscopic picture of "cherry-red spot" in an adult with the myoclonic syndrome.

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ژورنال

عنوان ژورنال: Journal of Movement Disorders

سال: 2009

ISSN: 2005-940X,2093-4939

DOI: 10.14802/jmd.09014