The results of this investigation can, in part, be explained by anatomical discrepancys between the hemispheres. In 1968, Norman Geschwind and Walter Levitsky gear up that in most brains the upper sur verbalism of the temporal lobe, or the planum temporale, is larger in the left hemisphere than in the right. This difference is related to the fact that, in most people, speech and linguistic process control is often located in that hemisphere.
In other study on splitbrain patients, a undecided was shown pictures of different faces put together to form one composite face: half of one face would be on one side of the dot, and half of another face would be on the opposite side. When a picture was flashed of a woman's face on the left side of the dot, and a child's face on the right, the patient consistently answered that she had seen the picture of th
Currently, no treatment for Huntington's sickness exists. Some progress is being made though towards elucidating its pattern of inheritance. A test whitethorn soon enable investigators to target the defective gene.
However, when the patient was asked to meridian to the picture she had seen, she tended to point to the woman wearing glasses. This is because the information from her left visual field was processed by her right, nonspeaking window dressing hemisphere.
Alzheimer's disease has features in common with both Parkinson's and Huntington's diseases. kindred Parkinson's disease, Alzheimer's involves alteration in brain biochemistry; specifically it is associated with acquittance of neurotransmitters within the cerebral cortex. In addition, as with Huntington's disease, the disorder whitethorn also be inherited.
e child. The information processed in her left hemisphere was evidenced by her left brain language response.
What treatments are useful in treating degenerative disease?
Another degenerative brain disease, Huntington's disease, was first described by George Huntington. Dr. Huntington's analyses of the disorder were based on cases that he himself, his father, and his grandfather in the first place him had observed in their practices. The condition generally develops in patients in their late 30's and early 40's. It is an inherited disorder passed from one contemporaries to the next according to autosomal dominant transmission. Initial symptoms include mild mental problems such as forgetfulness and outbursts. Behavioral symptoms therefore generally progress to movement problems (i.e., uncon
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