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1) fertilization 2) cell division 3) blastocyst formation |
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How long does each of the 3 developmental stages last? |
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1) pre-embryonic (conception to 2 weeks) 2) embryonic (2-8 weeks) 3) fetal (9 weeks-birth) |
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- begins in embryonic stage - outer layer: ectoderm (gives rise to NS) - middle layer: mesoderm (gives rise to muscles, skeleton, excretory & circulatory systems, and dermis) - inner layer: endoderm (develops into visceral organs like liver, pancreas, and respiratory system) |
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What occurs during the fetal stage of development? |
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Brain and cellular level development continue til birth to divide into a systematic nervous system and also in neo natal stages |
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1) longitudinal thickening of the ectoderm = neural plate 2) folding of the edges of the plate = neural groove 3) folds touch = neural tubes 4) ends of tube = neuropores 5) adjacent and other ectodermal cell form = neural crest |
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Superior vs. inferior neuropore |
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Superior = brain development Inferior = Spinal cord development |
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What part of the nervous system does the neurotube create? |
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Neural tube differentiates into what layers |
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1) marginal layer 2) mantle layer |
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- outer wall - contains processes of cell bodies present in mantle layer - becomes white matter in fetal stage (contains axons and glial cells) |
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- inner wall - becomes gray matter in fetal stage (contains cell bodies) - cells proliferate for form grooves on each side of the tube separating it into the ventral and dorsal sections |
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- spherical cell clusters from the division of the mesoderm - created as the inferior neuropore closes |
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Divisions of the mantle layer |
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- ventral and dorsal - ventral (motor plate/basal plate, gray matter derived from basal plate become ventral horns) (motor) - dorsal (association plate/alar plate, gray matter derived from association is called the dorsal horn) (sensory) |
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neurons differentiate after migrating to their final location |
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- neurons send a process to the brain surface to lift themselves - climbing along radical glia |
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outgrowth of axons and guidance of growth cone |
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- samples the environment contacting cells and chemical cues |
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- once the growth cone contacts its target cell then synaptic vesicles soon form |
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Lifelong changes in synapses |
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- the development of neurons is partially dependent on activities |
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1) hindbrain: includes cerebellum, pon, and medulla 2) midbrain: meseocencephalon (associated with vision, hearing, motor control, temp regulation). Composed of tectum, tegmentum, and cerebral peduncle 3) forebrain: cerebrum, thalamus, hypothalamus, limbic system |
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cranial part of the neural tube fail to develop -anencephaly -arnold-chiari malformation |
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-Formation of brainstem without cerebral and cerebellar hemispheres -occurs when the cranial end of the tube remains open and the forebrain does not develop -skull doesn't form or it is an incomplete brain leaving a malformed brainstem and the meninges exposed |
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Arnold-Chiari Malformation |
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-developmental deformity of the hindbrain -type I: not associated with defect of lower neural tubes both medulla and pons are small and deformed -type II: consist of malformation of brainstem and cerebellum leading to extension of medulla and cerebellum through the foramen magnum |
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Neural tube defects of SC |
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-caused by incomplete closing of the embryonic neural tube -spinabfida occulta -spinabfida meningoceole -spinabfida meningomyelceole -spinabfida myeloschisis |
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-mildest form of spinabfida -neural tissue does not protrube the bone -spinal function is normal -often asymptomatic |
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-protrusion of meninges through bony defect -may be asymptomatic -spinal cord function is impaired |
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Spinabfida meningomyeloceole |
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-meninges protrude outside of the body -results in abnormal growth of the spinal cord and some degree if lower extremity dysfunction -often bowel and bladder control is impaired |
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-most severe defect -consists of malformed spinal cord open to the surface of the body -occurs when neural folds fail to close |
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-forebrain malformation -mental retardation -neuronal migration -cerebral palsy |
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-olfactory -sensory nerve -location: inferior frontal lobe -function: smell -related disorders: lesion, inability to smell (anosmis) |
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-optic -sensory nerve -location: diencephalon -function: vision -related disorders: blindness and loss of pupillary reflex |
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-oculomotor -mixed nerve -location: anterior midbrain -function: control of eyelid muscles and eyeball rectus muscles -related disorders: lesion, inability to smell (anosmis) |
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-trochlear -motor nerve -location: posterior midbrain -function: activation and control of superior oblique muscle of eyeball -related disorders: no control on function if damaged |
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-trigeminal -mixed nerve -location: lateral pons -function: innervates muscles of mastigation, sensory on ipsilateral side -related disorders: sensory on ipsilateral side will be lost, problems in lower jaw movement |
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-abducens -motor nerve -location: between pons and medulla -function: control of lateral rectus muscles (eyes) -related disorders: paralysis of lateral rectal muscles (won't move and stays in one place) |
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-facial -mixed nerve -location: between pons and medulla -function: innervates ipsilateral facial muscles and sensory to anterior 2/3rd of tongue (sweet sensation) -related disorders: Bell's palsy |
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-vestibulocholclear -sensory nerve -location: between pons and medulla -function: gaze fixation to carry information of head movement and position to the brain, hearing information translation -related disorders: differences in head movement and gave fixation, balance, hearing (can lead to deafness) |
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-glossopharyngeal -mixed nerve -location: medulla -function: sensory to posterior 1/3rd of tongue (bitter) and gag reflex, innervates pharyngeal muscles -related disorders: swallowing difficulty, saliva decreased |
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-vagus -mixed nerve -location: medulla -function: motor to gag reflex and speech production and sensory to parasympathetic control -related disorders: difficulty speaking/swallowing |
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-spinal accessory -mixed nerve -location: medulla and spinal cord -function: innervates sternocleidomastoid muscles and trapezius muscles -related disorders: paralyzes sternocleidomastoid and trapezius muscles |
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-hypoglossal -mixed nerve -location: medulla -function: innervates tongue muscles -related disorders: dysphasia (difficulty swallowing) |
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rapid involuntary motor responses to an environmental stimulus detected by sensory receptors |
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includes sensory receptor sensory neuron, integrating center, motor neuron and effector cell |
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-two vertebral arteries enter the brain from the caudal region in the medulla -supply blood to medulla and inferior cerebellum -branches into anterior and posterior spinal arteries and posterior inferior cerebellar artery |
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-the vertebral arteries join near pontomedullary junction to form basilar artery -supply blood to the pons and most of cerebellum and medulla -branches into anterior inferior cerebellar artery and posterior cerebral artery |
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-enters the skull through the temporal bones -supplies blood to the cerebrum along with the poterior cerebral artery -branches into anterior and posterior communicating arteries, anterior and middle cerebral arteries |
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consists of: -1 anterior communicating artery -2 anterior cerebral arteries -2 internal carotids -2 posterior communicating -2 posterior cerebral arteries |
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