Family Myoclonus.

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Myoclonus and Ataxia Occuring in a Family.

[n 1914 J. Ramsay Hunt described the syndrome he called 'dyssynergia cerebellaris progressiva'. He regarded this condition with its well-defined cerebellar symptoms as an 'organic disease caused by degeneration of certain special structures of the cerebellar mechanism'. In 1921 at an annual meeting of the American Neurological Association, he presented a further six cases which combined the sym...

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Spinal myoclonus.

A case of rhythmic myoclonus affecting only the lower part of the body is described. This occurred as an acute self-limiting illness. The changes in the cerebrospinal fluid (CSF) suggested a viral infection. Clinical and electrophysiological findings indicated that the involuntary movements were arising at spinal level and were independent of suprasegmental influences. There are few previously ...

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Uraemic myoclonus: an example of reticular reflex myoclonus?

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Brachial plexus myoclonus.

Rhythmic myoclonus in an arm began abruptly following an injury and persisted continuously for six years. Topographical EMG showed abnormal activity confined to muscles innervated by the axillary and radial nerves from the posterior cord of the brachial plexus. Abduction of the arm above horizontal level stopped myoclonus and EMG discharges. EEG was normal. It is suggested that the myoclonus wa...

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Quetiapine Induced Myoclonus

Miss D, a 19-year-old female presented to us with history suggestive of manic episode for the last 2 months. Her past history also revealed history of 2 GTCS around 6 years back for which no treatment was sought. Her family and personal history were non signiÞ cant. She was started on quetiapine gradually increased to 300 mg per day over a week and lorazepam 2 mg at night. She showed improvemen...

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ژورنال

عنوان ژورنال: Proceedings of the Royal Society of Medicine

سال: 1913

ISSN: 0035-9157

DOI: 10.1177/003591571300600807