“…The mode of inheritance appears to be by an autosomal dominant gene of incomplete penetrance. DISCUSSION Since the original description by Ramsay Hunt in 1914, Wohlfart andHook (1951), Gilbert et al (1963), Aigner and Mulder (1960), Bradshaw (1954), Noad and Lance (1960), and Harriman and Millar( 1955) have described a variety of syndromes in-F cluding dyssynergia, myoclonus, and epilepsy. The existence of a variant of the Ramsay Hunt syndrome, i.e., progressive cerebellar dyssynergia, myoclonus, and without epilepsy, was recognized by Ramsay Hunt (1921), Wohlfart and Hook (1951), and Gilbert et al (1963), and is unlike the disorder described by Unverricht (1891) and Lundborg (1903) because of the absence of mental deterioration and epilepsy.…”