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Vocabulary-based flashcards covering nervous system anatomy, stroke mechanisms, seizure types, and neurodegenerative disorders such as Parkinson's, ALS, and Alzheimer's.
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Frontal lobe
Responsible for personality, judgment, voluntary movement, and expressive speech.
Parietal lobe
Brain region that processes sensation.
Temporal lobe
Brain region that supports hearing, language, and memory.
Occipital lobe
Brain region that processes vision.
Reticular activating system (RAS)
The system responsible for maintaining alertness.
Aphasia
Impaired ability to speak, understand, read, or write because of damage to the brain's language areas.
Expressive or Broca Aphasia
Difficulty producing words while understanding language remains intake, caused by damage to the frontal lobe.
Receptive or Wernicke Aphasia
Condition where a person speaks fluently but the words may not make sense, caused by damage to the temporal-parietal region.
Global Aphasia
Severe impairment in both understanding and producing language due to extensive damage involving both major language areas.
Cushing triad
A late and dangerous sign of increased ICP consisting of increased systolic BP/widened pulse pressure, bradycardia, and irregular respirations.
Papilledema
Blurred vision caused by pressure transmitted to the optic nerve.
Bitemporal hemianopia
Loss of lateral vision from both visual fields, often associated with pituitary tumors.
Ataxia
Loss of coordination and balance problems typically associated with cerebellum or brainstem manifestations.
Transient Ischemic Attack (TIA)
A temporary interruption of blood flow that causes stroke symptoms which resolve within minutes, leaving no permanent infarction.
Thrombotic stroke
The most common type of stroke, occurring when a clot forms in a cerebral artery, usually over atherosclerotic plaque.
Embolic stroke
A stroke where a clot travels from another location to block a cerebral artery.
Hemorrhagic stroke
A stroke caused by the rupture of a cerebral blood vessel, resulting in high ICP and potential herniation.
Ischemic stroke
A broad category including thrombotic and embolic strokes that account for about 87% of strokes.
Penumbra
The surrounding tissue of an infarcted central area in an ischemic stroke that may be saved with rapid treatment.
Apraxia
Difficulty planning movements, often seen in left frontal and parietal strokes.
Shingles
Reactivation of varicella-zoster virus producing a painful, blistering rash in a dermatomal pattern.
Ptosis
A drooping eyelid.
Agnosia
The inability to recognize everyday objects.
Contralateral
A term referring to the opposite side.
Dysarthria
Difficulty pronouncing words.
Paraplegia
Paralysis of the lower half of the body.
Photophobia
Increased sensitivity to light.
Quadriplegia
Paralysis of all four limbs.
Ipsilateral
A term referring to the same side.
Hemiplegia
Paralysis of one side of the body.
Glioma
A brain tumor originating in neurologic cells.
Contusion
Bruising of the brain.
Absence or Petit Mal Seizure
A brief staring episode usually lasting less than 20seconds without major collapse or postictal confusion.
Prodromal signs
Nonspecific changes such as irritability or headache occurring hours or days before a seizure.
Aura
A specific sensation that occurs immediately before or at the beginning of a seizure.
Tonic Phase
A phase of a seizure where the body becomes stiff and the person loses consciousness.
Clonic Phase
A phase of a seizure characterized by repetitive rhythmic jerking.
Parkinson's Disease
A disorder caused by the degeneration of dopamine-producing neurons in the substantia nigra.
Bradykinesia
Slowness of movement, characteristic of Parkinson's Disease.
Lewy bodies
Abnormal structures containing alpha-synuclein that may be present in Parkinson's Disease.
Amyotrophic Lateral Sclerosis (ALS)
A progressive, fatal disease involving degeneration of upper and lower motor neurons, resulting in muscle atrophy and respiratory failure.
Myasthenia Gravis
An autoimmune disorder where antibodies target ACh receptors, causing fluctuating muscle weakness that improves with rest.
Huntington's Disease
An autosomal dominant mutation involving an expanded CAG repeat in the HTT gene, leading to chorea and cognitive decline.
Beta-amyloid plaques
Typical brain changes in Alzheimer's Disease found between neurons.
Tau neurofibrillary tangles
Typical brain changes in Alzheimer's Disease found inside neurons.