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37 Cards in this Set

  • Front
  • Back
violent sequence of uncontrollable muscular movements caused by a seizure
Convulsions
A seizure that begins at a FOCUS and remains localized, not generalizing to the rest of the brain
PARTIAL seizure
Type of seizure disorder characterized by periods of inattention which are not subsequently remembered; also called a PETIT MAL seizure
Absence
A cerebrovascular accident caused by the rupture of a cerebral blood vessel
Hemorrhagic stroke
A generalized tonic-chlonic seizure that results in a convulsion
Grand mal
A cerebrovascular accident caused by occlusion of a blood vessel
Obstructive Stroke
Seizure that involves most of the brain as opposed to a localized area
GENERALIZED seizure
the interruption of the blood supply to a region of the body
Ischemia
A condition in which a patient undergoes a series of seizures without regaining consciousness
STATUS EPILEPTICUS
Seizure that starts from a focus, remains localized, but does not produce loss of consciousness
Simple partial seizure
Blood clot that forms within a blood vessel, which may occlude it
Thrombus
The phase of a grand mal seizure in which the patient shows rhythmic jerking movements
CLONIC phase
a peice of matter such as a blood clot, fat, or bacterial debris that dislodges from its site of origin and occludes an artery;
Embolus
seizure that starts from a focus and remains localized and produces a loss of consciousness
Complex Partial Seizure
hereditary disorder caused by the absence of an enzyme that converts phenylalanine to tyrosine
Phenyketonuria
found in the nigrostriatal neurons in people with Parkinsons disease
Lewy Body
the first phase of a grand mal seizure in which all of the patients skeletal muscles are contracted
The TONIC phase
heritable fatal METABOLIC STORAGE disorder; lack of enzymes in lysosomes causes accumulation of waste and produces swelling of cells of the brain
Tay-Sachs Disease
Said of a genetic disorder caused by a dominant mutation that involves a faulty gene that produces a protein with toxic effects
Toxic Gain of Function
disorder caused by the presence of an extra twenty first chromosome
Down syndrome
Contagious brain disease whose degenerative process gives the brain a SPONGELIKE appearance; caused by accumulation of misfolded PRION protein
Transmissable Spongiform Encephalopathy
protein that plays a role in ferrying defective or misfolded proteins to the proteasomes. mutated, it is a cause of familial Parkinsons disease
Parkin
lack of enzymes in lysosomes causes accumulation of waste and produces swelling of cells of the brain
Tay-Sachs Disease
Protein normally found in the PRESYNAPTIC membrane, where it is apparently involved in synaptic plasticity.
Alpha-Synuclein
a protein that can consist in TWO FORMS that differ only in their three dimensional shape;
PRION
abnormal accumulations of ________ are apparently the cause of neural degeneration in Parkinsons disease
Alpha Synuclein
Killer enzyme that plays a role in apoptosis
Caspase
Said of a genetic disorder caused by a recessive gene that fails to produce a protein that is necessary for good health
Loss of Function
protein that attaches itself to faulty or misfolded proteins and thus targets them for destruction by roteasomes
Ubiquitin
Organelle responsible for destroying defective or degraded proteins within the cell
Proteasome
abnormal circular structures with a dense core consisting of alpha-synuclein protein; found in the nigrostriatal neurons in people with Parkinsons disease
Lewy Body
inherited disorder that causes degeneration of the basal ganglia
Huntingtons disease
protein that may serve to facilitate the production and transport of brain derived neurotrophic factor.
Huntingtin (htt)
disorder characterized by progressively more severely uncontrollable jerking movements, writhing movements, dementia, and finally death
Huntingtons disease