Week 1:2 Flashcards

1
Q

3 stages of development in utero

A
  • pre-embryonic
  • embryonic
  • fetal
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2
Q

pre-embryonic stage

A

conception to day 14

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3
Q

embryonic stage

A

day 15 to end of week 8

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4
Q

fetal stage

A

week 8 to birth

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5
Q

ectoderm becomes

A
  • neurons and skin

- gives rise to nervous system

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6
Q

endoderm becomes

A

some internal systems and linings of tracts

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7
Q

When must the neural tube close?

A

between days 14 and 28

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8
Q

What is taken to prevent spina bifida?

A

folic acid

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9
Q

When does the neural plate form?

A

day 16

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10
Q

When does the neural tube form?

A

day 18

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11
Q

What happens on day 21?

A
  • neural tube almost closed

- development of neural crest

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12
Q

How does the neural tube form?

A

top down

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13
Q

Where do the neural folds fuse?

A

at the cervical spinal cord

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14
Q

Day 24 significance

A
  • top closes

- development of primary vesicles

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15
Q

Day 28 significance

A

bottom closes

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16
Q

What do primary vesicles give rise to?

A

parts of the nervous system

  • prosencephalon
  • mesencephalon
  • rhombencephalon
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17
Q

What does the prosencephalon give rise to by week 6?

A
  • telencephalon

- diencephalon

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18
Q

What does the telencephalon eventually become?

A
  • cerebral hemispheres

- lateral ventricles

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19
Q

What does the diencephalon eventually become?

A
  • thalamus
  • hypothalamus
  • retina
  • third ventricle
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20
Q

What does the mesencephalon become?

A
  • midbrain

- cerebral aqueduct (aka fourth ventricle)

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21
Q

What is the midbrain part of?

A

brainstem

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22
Q

What does the rhombencephalon become by week 6?

A
  • metencephalon

- myelencephalon

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23
Q

What does the metencephalon become?

A
  • pons

- cerebellum

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24
Q

What does the myelencephalon become?

A

medulla

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25
What do the metencephalon and the myelencephalon help to form?
fourth ventricle
26
What occurs with failure of the neural tube to close?
morphogenesis
27
failure of closure of ANTERIOR (rostral) neuropore
anencephaly
28
anencephaly
- large portions of scalp, cranial bones, and cerebral hemispheres are absent - most die in utero, virtually all by first postnatal week, very few survive
29
failure of closure of POSTERIOR (caudal) neuropore
spina bifida
30
two types of spina bifida
- oculta | - cystica
31
spina bifida oculta
- virtually no clinical signs | - tuft of hair on lumbar region
32
spina bifida cystica
herniation through the vertebral area
33
2 forms of spina bifida cystica
- spina bifida with meningocele | - spina bifida with myelomeningocele
34
spina bifida with meningocele
- herniation of the meninges, but no neural structures through the vertebral defect - may be without symptoms
35
spina bifida with myelomeningocele
protrusion of both the spinal cord and meninges
36
symptoms of spina bifida with myelomeningocele
- saddle anaesthesia - paralysis of bladder and bowel sphincters - paralysis of lower limbs
37
When is the CNS the most susceptible to major malformations?
between day 14 and week 20
38
implications of developmental disorders
- growth and remodeling continue, but later insults can cause functional disturbances and/or minor malformation
39
hydrocephalus
- excessive buildup of CSF | - compression of brain and expansion of skull due to increased intracranial pressure
40
What might cause excessive buildup of CSF?
- blockage of foramen | - primary condition or secondary to other disease
41
treatment of hydrocephalus
drained by surgically implanted shunts
42
cerebral palsy
non-progressive motor disorder of prenatal, during childbirth, or shortly after birth
43
What are more cases of cerebral palsy due to?
stroke or anoxia from complications of pregnancy (infection, poor nutrition, late pregnancy, prematurity)
44
How is cerebral palsy classified?
by motor dysfunction (even if with problems of sensation, cognition, or language
45
types of cerebral palsy
- spastic - dyskinetic - ataxic
46
part of brain involved: spastic
cerebral cortex
47
part of brain involved: dyskinetic
basal ganglia
48
part of brain involved: ataxic
cerebellum
49
How is spastic CP classified?
by the extent of impairment
50
types of spastic CP
- hemiplegic - diplegic - quadriplegic
51
hemiplegic spastic CP
one side affected
52
diplegic spastic CP
both LE affected
53
quadriplegic spastic CP
all limbs affected
54
focus of treatment for CP
- improving functional abilities - reducing impairments PT: stretching to improve ROM, prevent contractures, developing WB MD: reducing spasticity with drugs or surgery
55
What does the notochord do?
helps form the vertebral column
56
What do somites form?
most of the skull, spinal column, and supporting structures (surrounding skeletal muscles, segmentation of spinal cord)
57
spina bifida correction
correctible with surgery, but spina bifida with myelomeningocele may have motor delays
58
What does cerebral palsy largely affect?
motor cortex
59
spasticity
continued contraction of muscles
60
dyskinetic
problems with voluntary movement and motor planning
61
What are contractures caused by in people with cerebral palsy?
spasticity