embryologic development Flashcards

1
Q

otocyte

A

egg

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2
Q

mitosis

A

cell division

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3
Q

gastrulation

A

creation of the germ layers
-all growth is the result of cell division of preexisiting cells

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4
Q

3 germ layers

A

ectoderm, mesoderm, endoderm

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5
Q

ectoderm

A

outer skin layers, nervous system and sense organs
-early neural groove leads to entire CN
-the part that gets pinched off from the outside becomes the nervous system and CNS

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6
Q

mesoderm

A

skeletal structures, circulatory structures, meninges, notochord, reproductive organs and cartilage
-including ossicles and temporal bone
-in between two other germ layers

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7
Q

endoderm

A

digestive canal and respiratory organs (viscera)
-including middle ear, mastoid cavities, and ET
-most internal

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8
Q

neurulation

A

neural tube development
-within third week the ectoderm thickens to form the neural plalte
-fold inward forming a groove at midline with a fold on both sides
-neural folds begin to fuse midway along the groove which forms the tube
-fusion occurs along the tube (zipper action)
-then the tube separates from the surface ectoderm and is enclosed inside the body

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9
Q

spina bifida

A

failure of the caudal neuralpore to close
-vertebrae does not form over the spinal cord
-more route for infection

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10
Q

crania bifida

A

failure of the rostral neuropore (end of neural tube) to close
-central cavity is exposed
-not conductive to postnatal life

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11
Q

notochord

A

lies outside of the neural tube near the ventral surface and is the precursor for the skeletal axis, helping to form the vertebral column

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12
Q

crest cells

A

what is left behind by each neural fold
-forms sensory neurons of the dorsal root ganglia, some CN, postganglionic neurons of the autonomic nervous system, and schwann cells of the PNS

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13
Q

sulcus limitans

A

longitudinal groove in the lateral wall of the neural tube, separating the dorsal/alar half from the ventral/basal half in the future spinal cord and brainstem

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14
Q

ventral/basal division

A

anterior (ventral) horns in gray matter with somatic and autonomic motor neuron cell bodies

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15
Q

dorsal/alar division

A

posterior dorsal horns in the gray matter with ascending pathway cells

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16
Q

flexures of neural tube

A

cervical, cephalic, and pontine

17
Q

cervical flexure

A

where future brainstem meets future spinal cord
-straightens out through development

18
Q

cephalic flexure

A

at the level of the future midbrain and remains as the bend between the axis of the brainstem and the axis of the cerebrum in the adult CNS
-making a T shape meeting point

19
Q

pontine flexure

A

on the posterior/dorsal surface in the area of the pons and 4th ventricle

20
Q

secondary vesicles

A

encephalon, diencephalon, metencephalon, and myelencephalon

21
Q

telencephalon

A

cerebrum/cerebral hemispheres
-lateral ventricles
-comes off the prosencephalon (primary vesicle)

22
Q

diencephalon

A

thalamus (and hypothalamus and surrounding)
-third ventricle
-comes off the prosencephalon (primary vesicle)

23
Q

mesencephalon

A

midbrain
-forms cerebral aqueduct

24
Q

metencephalon

A

cerebellum and pons
-part of 4th ventricle
-comes off the rhombencephalon (primary vesicle)

25
myelencephalon
medulla -part of 4th ventricle and central canal -comes off the rhombencephalon (primary vesicle)
26
monogenic deficits
single mutant gene, mendelian inheritance pattern
27
multifactorial deficits
mendelian inheritance pattern, exogenous environmental factors -multiple things caused it
28
mitochondrial deficits
alteration in mitochondrial DNA, nonmendelian -mainly maternal transmission -affects enzymes of mitochondria
29
nonmendelian chromosomal aberrations
excess, lack or structural alteration of one or more of the 23 pairs of chromosomes -i.e. down syndrome
30
what ways can infants be assessed for abnormal functions
monitoring of infants -respiration -control of body temp -regulation of thirst and appetite -rooting -sucking, swallowing and grasping -movements and postures of neck, trunk, and limbs
31
tay-sachs disease
lysosomal storage disease -inability to break down ganglioside which accumulates in neurons causing them to swell or burst
32
niemann-pick disease
autosomal recessive inheritance -inability to break down sphingomyelinase which accumulates in neurons causing them to swell and burst
33
what do the germ layers become in AVS
ectoderm : outer and inner ear, membranous labyrinth mesoderm : ossicles, temporal bone, and bony labyrinth endoderm : middle ear epithelial lining, mastoid cavities and eustachian tube
34
branchial/pharyngeal arch structures
arches - external humps clefts/grooves - external pouches - internal membrane - point of contact of the groove and pouch
35
what do the archs become
first arch - rise to CN 5 second arch - rise to CN 7 third arch - rise to CN 4 fourth arch - rise to CN 10 sixth arch - rise to CN 11