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An in-depth exploration of the frontal lobe, focusing on its various functions, including motor control, eye movements, and executive functions. It discusses the sources of cortical neurons that project to the brainstem and spinal cord, the inputs and outputs of different areas such as M1, premotor cortex, frontal eye fields, and dorsolateral prefrontal cortex. Damage to these areas can result in various neurological deficits, such as apraxia, difficulty in using sensory feedback, and disinhibition.
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with the rest of the brain are complex and beyond the scope of this discussion. Damage to the frontal eye fields will cause deficits in voluntary eye movement to the contralateral visual field (leading to active visual search deficits), but preserved passive eye movement (as in the following of a moving object).
a. Figural fluency tasks: Patients are asked to draw as many different shapes as possible within a limited time period. Patients with dorsolateral dysfunction might get “stuck” on one shape and continue to draw either the same figure or something very similar (an error called perseveration ). Here one can observe that the patient is having difficulty generating multiple response alternatives.
b. Luria’s Alternating Figures Test: Patients are asked to copy a sequence of alternating +’s and 0’s and then to continue the pattern across the page (top image). Patients with dorsolateral dysfunction may persist in drawing only +’s or only 0’s (perseveration), or they may change the task entirely and begin drawing x’s (exhibiting impersistence in completion of the appropriate task). Again one can note difficulty in generating appropriate responses to the task at hand. Note that similar tests to assess errors of this sort may be performed using alternating hand movements or the drawing of different patterns of peaks and valleys (bottom image).
Frontal Cortex ± Striatum ± Globus Pallidus/Substantia Nigra ± Thalamus ± Frontal Cortex
fist when the examiner says “stop” and not tap when the examiner says “go”). A patient with orbitofrontal dysfunction will have difficulties inhibiting their behavior during these tasks.
The frontal cortex has connections to subcortical structures such as the thalamus and basal ganglia that function in regulation of behavior. As alluded to earlier, the dorsolateral prefrontal cortex is a part of a circuit with input from the thalamus and output to the striatum (a basal forebrain nucleus). The striatum then projects to globus pallidus/substantia nigra (another basal forebrain structure), which projects to the thalamus to complete the circuit. Other parallel but distinct connections exist between the orbitofrontal/cingulate frontal regions and their corresponding subcortical structures. In a very general sense, the frontal:subcortical:frontal circuits may be thought of a “filter” that serves to modulate the output of the frontal cortices to regions of the brain involved in motor control of behavior. Small subcortical lesions that affect any one of these circuits can mimic large cortical lesions.
Disorders Associated with Frontal Lobe Dysfunction
Frontal lobe dysfunction may be found in a host of disorders ranging from cortical degenerative disorders often seen in the elderly, including Alzheimer’s Disease and Fronto-Temporal Lobar Dementia, to disorders of a psychiatric nature (schizophrenia, obsessive compulsive disorder). As noted above, subcortical damage can also result in frontal dysfunction; such damage may be seen in disorders of basal ganglia nuclei such as Huntington’s Disease and Parkinson’s Disease. Some representative examples of disorders associated with frontal lobe dysfunction are as follows:
The deficits associated with frontotemporal dementia (FTD) may be contrasted with
essential nutrients). The disease is characterized by severe amnesia and causes degeneration of the medial thalamus, mamillary bodies, and cerebral atrophy in regions such as the frontal lobes (see image below). Patients with Korsakoff’s dementia often exhibit many of the same neuropsychological deficits that are seen in other frontal patients.