hereditary OPCA is caused by the inheritance of a defective gene. Several genes have been identified. The two most common are known as SCA-1 and SCA-2 (SCA stands for spinocerebellar ataxia ).
a group of disorders characterized by degeneration of three brain areas: the inferior olives, the pons, and the cerebellum . OPCA causes increasingly severe ataxia (loss of coordination) as well as other symptoms.
Olivopontocerebellar atrophy (OPCA) is a group of disorders characterized by degeneration of three brain areas: the inferior olives, the pons, and the cerebellum .
The average age of onset is 28 years.
Hereditary OPCA affects approximately 10,000 people in the United States, with males affected approximately twice as often as females.
The most common early symptom of OPCA is ataxia, or incoordination, which may be observed in an unsteady gait or over-reaching for an object with the hand.
The life expectancy after diagnosis is approximately 15 years, although this is an average and cannot be used to predict the lifespan of any individual person.
Hereditary OPCA, also called inherited OPCA and familial OPCA, is caused by inheritance of a defective gene, which is recognized in some forms but not in others.
An initial diagnosis of OPCA can be made with a careful neurological examination (testing of reflexes, balance, coordination, etc.), plus a magnetic resonance image (MRI ) of the brain
common symptoms include dysarthria (speech difficulty), dysphagia (swallowing difficulty), nystagmus (eye tremor), and abnormal movements such as jerking, twisting, or writhing. Symptoms worsen over time.
She has a muscular atrophy.
Atrophy is the wearing away of an organ or tissue because of lack of use. Bone Atrophy, obviously, is atrophy of bones.
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There are no perfect rhymes for the word atrophy.