Atypical spasmus nutans as an initial sign of thalamic neoplasm

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Latent nystagmus and acquired pendular nystagmus masquerading as spasmus nutans.

SUMMARY We used ocular motility recordings to identify the characteristics of a rare combination of conjugate, horizontal jerk, and pendular nystagmus in a 9-year-old boy. The clinical diagnoses were amblyopia, left esotropia, congenital nystagmus, and an apparently uniocular pendular nystagmus that mimicked spasmus nutans. Ocular motility recordings revealed an unusual latent/manifest latent n...

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Spasmus nutans. A quantitative prospective study.

Spasmus nutans includes ocular oscillations, head nodding, and anomalous head positions. No quantitative longitudinal study verifying the natural history of this self-limited condition has appeared in the literature. Using infrared oculography, we prospectively examined the eye movements of otherwise neurologically normal infants in whom a diagnosis of spasmus nutans had been made. At this writ...

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A study of head and eye movement in spasmus nutans.

A case of spasmus nutans was studied using objective recordings of head and eye displacement in order to generate a precise description of the ocular oscillations and head nodding and to investigate their interrelationships. The ocularoscillations consisted of 11-Hz sinusoidal convergence movements. The head nodding consisted of a 3-Hz, 3 degrees peak to peak, sinusoidal oscillation in the hori...

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Atypical vessels as an early sign of intracardiac myxoma?

We report on a woman with previously unknown left atrial myxoma, who underwent percutaneous coronary intervention. 45 months after the initial coronary angiography, echocardiography demonstrated a large atrial myxoma, which was not seen echocardiographically before. The retrospective analysis of the pre-intervention coronary angiography revealed atypical vessels in the atrial septum, which are ...

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Spasmus nutans and congenital ocular motor apraxia with cerebellar vermian hypoplasia.

BACKGROUND Spasmus nutans and congenital ocular motor apraxia share clinical characteristics. However, their development in a patient with cerebellar vermian hypoplasia has not been previously described. OBJECTIVE To report spasmus nutans and congenital ocular motor apraxia in a child with cerebellar vermian hypoplasia. DESIGN Case report. SETTING Tertiary-care hospital. Patient A 7-year-...

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ژورنال

عنوان ژورنال: Pediatric Neurology

سال: 1986

ISSN: 0887-8994

DOI: 10.1016/0887-8994(86)90083-4