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Neurology, Infectious disease. Post-viral cerebellar ataxia also known as acute cerebellitis and acute cerebellar ataxia ( ACA) is a disease characterized by the sudden onset of ataxia following a viral infection. [ 1] The disease affects the function or structure of the cerebellum region in the brain.
Parinaud's syndrome is a constellation of neurological signs indicating injury to the dorsal midbrain. More specifically, compression of the vertical gaze center at the rostral interstitial nucleus of medial longitudinal fasciculus (riMLF). It is a group of abnormalities of eye movement and pupil dysfunction and is named for Henri Parinaud [ 6 ...
Spinocerebellar ataxia ( SCA) is a progressive, degenerative, [ 1] genetic disease with multiple types, each of which could be considered a neurological condition in its own right. An estimated 150,000 people in the United States have a diagnosis of spinocerebellar ataxia at any given time. SCA is hereditary, progressive, degenerative, and ...
Nystagmus as seen in a case of ocular albinism. The cause of pathological nystagmus may be congenital, idiopathic, or secondary to a pre-existing neurological disorder.It also may be induced temporarily by disorientation (such as on roller coaster rides or when a person has been spinning in circles) or by some drugs (alcohol, lidocaine, and other central nervous system depressants, inhalant ...
Varies by severity, severely disabled animals may be euthanized for humane reasons. Frequency. Varies by species and breed. Cerebellar abiotrophy (CA), also called cerebellar cortical abiotrophy (CCA), is a genetic neurological disease in animals, best known to affect certain breeds of horses, dogs and cats. It can also develop in humans.
This makes immediate recognition and response critical. Some of the most common symptoms of anesthesia intolerance include: Excessive salivation or drooling. Prolonged recovery time. Low blood ...
Opsoclonus myoclonus syndrome. Opsoclonus myoclonus syndrome ( OMS ), also known as opsoclonus-myoclonus-ataxia (OMA), is a rare neurological disorder of unknown cause which appears to be the result of an autoimmune process involving the nervous system. It is an extremely rare condition, affecting as few as 1 in 10,000,000 people per year.
Vomiting. Weight loss. High fever. Pneumonia in severe cases. In cases where the bacterium has caused a systemic infection, you may observe more critical and life-threatening symptoms, including ...