Cogan oculomotor apraxia

Cogan oculomotor apraxia: congenital oculomotor apraxia an absence or defect of horizontal eye movements, so that when the patient tries to look at an object off to one side, the head must turn to bring the eyes into line with the object and the eyes exhibit nystagmus; the cause is probably a brain lesion. Called also Cogan syndrome.

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Cogan oculomotor apraxia syndrome — Co·gan oc·u·lo·mo·tor aprax·ia, syndrome (koґgən) [David Glendenning Cogan, American ophthalmologist, 1908â€“1993] see under apraxia and syndrome … Medical dictionary
Cogan syndrome — Arteritis (also referred to as vasculitis) that involves the ear. This condition is called Cogan syndrome after the American ophthalmologist David Glendenning Cogan (1908 93) who first described it. Cogan syndrome features not only problems of… … Medical dictionary
ocular motor apraxia — oculomotor apraxia defective or absent voluntary eye movements, often owing to a brain lesion. It may be congenital (see Cogan oculomotor a.) or acquired as a result of a brain lesion or ataxia telangiectasia … Medical dictionary
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