3 - Development and Aging

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33 Terms

1
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When does development of the nervous system begin?

Day 18

2
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When does the neural tube begin to develop?

Day 21

3
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When should the neural tube be completely closed?

Day 24

4
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When does neural tube begin to form the fore-, mid-, and hindbrains?

Day 28

5
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What does the forebrain eventually become?

cerebral hemispheres, thalamus and the hypothalamus.

6
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The midbrain does not change significantly after prenatal development.

True

7
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What does the hindbrain eventually become?

pons, cerebellum, medulla and the spinal cord

8
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Migration

Neurons move into their proper location

9
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Differentiation

Cells acquire as specific function and structure

10
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What neurological disorders are associated failure of cells to differentiate?

Fetal alcohol syndrome and Down syndrome 

11
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Myelination

Occurs by oligodendroglia cells in CNS and Schwann cells in PNS

12
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When does myelination begin and when is it MOSTLY complete?

Begins around 20 weeks gestation and is mostly complete at 2 years

13
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What part of the brain is the last to myelinate and when does this occur?

The prefrontal cortex and around early adulthood (early to late twenties)

14
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Synaptogenesis

The process of synapse formation that takes place throughout life

  • Synapses are strengthened through firing (or use)

  • Neural pathways that are not fired (or used) do not form synaptic pathway

  • Early life is a critical period of where many synapses are created

15
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At birth, cranial nerves for smell and taste are fully myelinated, but the optic nerves are not.

True

16
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At birth, cranial nerves used for sucking and swallowing are myelinated, but other motor pathways are not.

True

17
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How does aging affect the brain?

  • Brain shrinks and myelin thins (synaptic function is less effective)

  • Less synapses, postsynaptic receptors, and dendrites

  • Substantia nigra secretes less dopamine (50%) between 20-60 yo

  • Blood flow decreases (23%) between 33 and 61 yo

18
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Anencephaly 

Results from incomplete closure of the cranial end of the neural tube

19
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Spina bifida occulta

Occurs with the spinal cord and cauda equina develop normally and are covered by skin, but the neural arches are incomplete

20
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Spina bifida cystica

Occurs when the vertebral arches fail to develop and a large sac of meninges protrudes from the back

21
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Epilepsy

A brain disorder characterized by repeated seizures (generalized or partial)

  • Brain becomes overexcited and fires random APs

  • Causes: genetics brain disorder, head trauma, tumors, strokes, CP

22
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Status Epilepticus

Toxic effects of overactivity and overheating

  • Can result in death

  • A generalized seizure that lasts over 30 mins or more

  • This is a medical emergency

23
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Periventricular leukomalacia 

Damage to the white matter next to the lateral ventricles that is caused by a lack of blood flow or decreased oxygen in the blood

  • Can cause motor deficits that affect the lower extremities

24
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Intraventricular hemorrhage

Bleeding into the ventricles of the brain

  • Results in varying degrees of motor impairment depending on the extent of the bleeding

  • Typically occurs before 30 weeks of gestation

25
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Cerebral Palsy

Nonprogressive motor disorder that occurs prenatally, during the birth process, or shortly afterwards

  • Causes: infection, lack of oxygen, intraventricular hemorrhage, premature birth, and brain injury

  • Classified by the type of motor dysfunction despite presence of other impairments such as sensation, language and cognition

26
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Spastic CP

  • Lesion: UMN

  • Motor S/S: Spastic paralysis

  • Nonmotor problems: Impairments in sensory, vison, and hearing languages, problems, cognitive, and musculoskeletal 

27
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Athetoid CP

  • Lesion: Basal ganglia

  • Motor S/S: Writhing movements

  • Nonmotor problems: Impairments in sensory, vison, and hearing languages, problems, cognitive, and musculoskeletal 

28
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Ataxic CP

  • Lesion: Cerebellum

  • Motor S/S: Ataxic

  • Nonmotor problems: Impairments in sensory, vison, and hearing languages, problems, cognitive, and musculoskeletal 

29
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Mixed CP

  • Lesion: Mixture of motor areas

  • Motor S/S: Spastic paralysis

  • Nonmotor problems: Impairments in sensory, vison, and hearing languages, problems, cognitive, and musculoskeletal 

30
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Down Syndrome

Genetic disorder that results from the presence of a 3rd copy of chromosome 21

  • Includes: disability and hypotonia

  • Smaller brains, fewer cortical neurons, and abnormally dendrites

  • Cerebellum contains many undifferentiated cells

31
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Autism

Pervasive development disorder

  • Characterized by social interaction and communication

  • Some people display stereotypical, repetitive behavior patterns and some cognitive impairments

  • Brain produces less serotonin than normal

  • Can have issue with movement (due to cerebellum)

32
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Hydrocephalus 

  •  Results from blockage of flow of CSF through the ventricles and subarachnoid space 

  • Swelling of the brain ventricles causes compression and damage to neural tissues

  • May occur in combination with spina bifida or Arnold-Chiari malformation

33
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What is the relation between nutrition, exercise and cognitive function?

  • Fitness is associated with better cognition, achievement and behavior, and fatness with worse scores

  • Executive function, mathematics and reading achievement, and parent ratings of child behavior were related to fitness and fatness.

  • The same is generally true for older adults (exercise can prevent or reduce age-related cognitive loss)