منابع مشابه
Hereditary chin trembling or hereditary chin myoclonus?
Hereditary chin trembling is a rare autosomal dominant disease often considered as an "essential tremor variant". The clinical and neurophysiological data obtained in a new white family lead to the suggestion that this abnormal involuntary movement is a focal variant of hereditary essential myoclonus.
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In 1930 Frey described an unusual involuntary movement of the muscles of the chin, inherited as a dominant characteristic through five generations. Ganner (1938) described a similar family, and in discussion Westphal (1938) mentioned a family in whom this trait could be followed through six generations. Grossman (1957) and Wadlington (1958) reported smaller affected families, and Ford (1960) me...
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ژورنال
عنوان ژورنال: Journal of Biological Chemistry
سال: 1935
ISSN: 0021-9258
DOI: 10.1016/s0021-9258(18)75010-2