Neurodegenerative Diseases Flashcards

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0
Q

Give the facts on Alzheimer’s?

A

Disease of ageing, memory loss and dementia

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1
Q

Give the four neurodegenerative diseases studies?

A

Alzheimer’s, Huntingdon’s, multiple sclerosis and Parkingson’s

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2
Q

Give a) early, b) later and c) late symptoms of Alzheimer’s?

A

A) short term memory loss, disorientation, clumsiness, problems with visuospatial orientation and words/numbers/names
B) loss of social skills, psychosis and paranoia, rigidity (bradykinesia)
C) mutism, incontinence and bedridden

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3
Q

What happens to the gyri and sulci in Alzheimer’s?

A

Gyri narrow and sulci widen

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4
Q

What part of the brain are majorly effected in Alzheimer’s?

A

The hippocampus

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5
Q

What proteins build up in Alzheimer’s?

A

Tau protein forms neurofibrillary tangles and amyloid ß protein forms plaques

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6
Q

Which pathways are particular effected and suffer from neuronal loss in Alzheimer’s?

A

Cholinergic pathways

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7
Q

How is Alzheimer’s treated?

A

Based on AChE inhibitors, try to increase acetylcholine levels which may slow progression and improve cognition

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8
Q

What are the symptoms of MS?

A

Sensory changes, muscle weaknesses, cooordination and balance, speech, swallowing, visual, fatigue, pain, incontinence, cognitive impairment, depression and mood swings.

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9
Q

What are the different forms of progression of MS?

A

Progressive-relapsing: steady decline with superimposed attacks
Secondary progressive: initial relapsing which suddenly become decline without relapses
Primary progressive: continuous decline with no attacks
Relapsing-remitting: unpredictable attacks lead by periods of remission

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10
Q

What is the cause of MS?

A

Oligodendrocytes are effected causes a degradation of the myelin sheath

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11
Q

What is parking sons disease?

A

An extrapyramidal disorder- loss of movement, shakiness and increased muscle tone

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12
Q

What are the symptoms of parkingsons disease?

A

Tremor, rigidity, speech problems, micrographia (tiny handwriting), akinesia, postural changes (stoop and shuffling)

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13
Q

What part of the brain is diminished in parkingsons?

A

The substantia nigra

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14
Q

What is Huntingdon’s disease?

A

An inherited, autosomal dominant disorder

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15
Q

What causes Huntingdon’s?

A

Polyglutamine repeat, huntingtin protein

16
Q

What are the symptoms of Huntingdon’s?

A

Irritability, moodiness, antisocial behaviour, fidgeting and restlessness

17
Q

Where are the loss of neurones in Huntingdon’s?

A

Cerebral cortex and corpus striatum