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There are two main aspects of gourmand syndrome: first, the fine dining habits and changes to taste, and second, an obsessive component which may result in craving and preservation. [2] Gourmand syndrome can be related to, and shares biological features with, addictive and obsessive disorders. [2] [3] The syndrome was first characterized in ...
Research involving lesions to the basolateral nucleus have shown a strong association with memories involving fear. The central nucleus is linked with the behavioral responses that are dependent on the basolateral's reaction to fear. [6] The central nucleus of the amygdala is also linked to emotions and behaviors motivated by food and sex. [7]
Diabetes is the leading known cause of neuropathy in developed countries, and neuropathy is the most common complication and greatest source of morbidity and mortality in diabetes. A systematic review has found that diabetic peripheral neuropathy affects 30% of diabetes patients. [ 1 ]
Multi-organ CT scans may help doctors identify those who may have a heightened risk of developing type 2 diabetes, a new study suggests. ... adults with an average age of 45 who received a CT scan ...
Redlich used the term 'miliary sclerosis' to describe plaques because he thought they resembled millet seeds, and he was the first to refer to the lesions as 'plaques'. [4] In the early 20th century, Oskar Fischer noted their similarity to actinomyces 'Drusen' (geode-like lesions), leading him to call the degenerative process 'drusige Nekrose ...
The uncinate fasciculus is a bi-directional pathway between the temporal lobe and frontal lobe; it is traditionally considered to be part of the limbic system. [2] It has been proposed that the uncinate fasciculus allows mnemonic representations stored in the temporal lobe to interact with and guide decision making in the frontal lobe.
Lesions to V1, for example, can cause blindsight in different areas of the brain depending on the size of the lesion and location relative to the calcarine fissure. [12] Lesions to V4 can cause color-blindness, [13] and bilateral lesions to MT/V5 can cause the loss of the ability to perceive motion.
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