PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “CEREBELLAR DISEASES”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 73 records · Page 4Linked to original sources

Paraneoplastic cerebellar disease. Remission with excision of the primary tumor.

We describe two patients with paraneoplastic cerebellar syndromes who gained clinically useful neurologic remissions following radical excision of the primary cancer. In both patients the syndrome was characterized by the rapid onset of gait ataxia, nausea, postural vertigo, central positional nystagmus, and saccadic oscillations. These observations encourage radical treatment of the primary cancer in patients with advanced malignant neoplasms who are disabled by cerebellar dysfunction, and lend support to a current hypothesis that paraneoplastic cerebellar degeneration is due to anticerebellar Purkinje cell antibodies elaborated by the primary cancer.

Adenocarcinoma↗

Gait disturbances in patients with labyrinthine and cerebellar diseases.

In order to clarify the peculiarities of gait disturbances appearing in patients with labyrinthine and cerebellar disturbances, the upward-downward (U-D), right-left (R-L) and forward-backward (F-B) movements of the head and activities of both soleus muscles were recorded by a polygraph and a data recorder with the aid of a five-channel telemeter. The power spectrum and correlation analyses were carried out with a PDP-11 computer. The following are results obtained from walking with the eyes closed. (1) On normal subjects, the power spectrum of U-D head movement indicated a rise at about 2 Hz. The autocorrelograms of U-D, R-L head movements and soleus muscle activities showed a chopping or sine wave process with an attenuation of amplitude. A cross correlogram revealed that when the head was inclined to the right side, the contralateral soleus muscle was active and when the head was inclined forward, one of the soleus muscles was active. (2) A patient with bilateral loss of labyrinthine function showed an increased R-L head sway and irregularly undulating F-B head movement, indicating disturbances of the labyrinthine righting and linear movement reflexes. (3) A patient with cerebellar atrophy indicated irregular U-D, R-L and F-B head movements. The soleus muscle activity changed irregularly.

Cerebellar Diseases↗

Non-motor associative learning in patients with isolated degenerative cerebellar disease.

In recent decades it has become clear that the cerebellum is involved in associative motor learning, but its exact role in motor learning as such is still controversial. Recently, a contribution of the cerebellum to different cognitive abilities has also been considered, but it remains unclear whether the cerebellum contributes to cognitive associative learning. We compared nine patients with an isolated cerebellar degenerative disease in a cognitive associative learning task with 10 controls. Patients and controls were matched for age, sex, handedness, level of education, intelligence and capabilities of visual memory. The subjects were asked to learn the association between six pairs of colours and numerals by trial and error. Additionally, a simple reaction time and a visual scanning test were conducted in order to control for the influence of motor performance deficits in cerebellar patients. In comparison with the controls, it took the patients significantly longer to learn the correct associations between colours and numerals, and they were impaired in recognizing them later on. Two patients showed no associative learning effect at all. Neither the simple reaction time nor the visual scanning time correlated substantially with the results of associative learning. Therefore, motor-associated disabilities are unlikely to be the reason for the learning deficit in cerebellar patients. Our results suggest that the cerebellum might contribute to motor-independent processes that are generally involved in associative learning.

Aged↗

Chronic mania in childhood: case report of a possible association with a radiological picture of cerebellar disease.

The case-history of a woman with psychiatric symptoms since childhood is reported, the best label for which was that of "chronic mania". Cerebellar atrophy was suspected on radiological grounds. The literature on chronic mania in childhood and on cerebellar damage and mental changes is reviewed and the view is put forward that cerebellar dysfunction may play a part in the production of some psychiatric symptoms.

Adult↗

Studies of eccentric gaze stability: effects of pitch head position on horizontal gaze-holding in patients with cerebellar disease.

We studied the effects of change of head position in the pitch plane on the ability to hold horizontal eccentric gaze in five patients with cerebellar disorders. All patient showed a change in the time constant of horizontal centripetal drift when the head was pitched forward or back. This result suggests that otolithic inputs can influence the neural integrator for horizontal eye movements and indicates the value of testing horizontal gaze holding in different head positions.

Cerebellar Diseases↗

Diagnostic approach to cerebellar disease in children.

We reviewed the clinical records of 51 extensively investigated pediatric patients with structural abnormalities of the cerebellum as revealed by magnetic resonance imaging (MRI). Ten had hypoplasia of the vermis, 21 had hypoplasia of the vermis and cerebellar hemispheres, 2 had pontocerebellar hypoplasia, and 18 had progressive cerebellar atrophy. A clear diagnosis was reached in 37 (72.5%). Initial characterization of the cerebellar alterations by MRI separated hypoplastic from atrophic cases and confirmed MRI as an essential preliminary means for distinguishing malformations from metabolic-degenerative conditions. However, the diagnostic possibilities are so numerous that it is not feasible to propose a standardized diagnostic protocol for pediatric patients with an altered cerebellum. Subsequent investigations should be suggested by the neuroradiologic and clinical peculiarities of each case.

Adolescent↗