ORGANIZATION AND DEVELOPMENT Flashcards

1
Q

Central Nervous System (CNS)

consists of?

is developed from?

A

CNS consists of the

BRAIN + SPINAL CORD

CNS is develop from the

NEURAL TUBE

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2
Q

PERIPHERAL NERVOUS SYSTEM (PNS)

consists of ?

derives from?

A

neurons which axons grow out of neural tube

+

neurons derived from neural crest

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3
Q

PNS

which neurons are derived from neural tube?

A

skeletal motor neurons

+

preganglionic autonomic neurons

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4
Q

PNS are formed by 12 pairs of cranial nerves and 30 pairs of spinal nerves

TRUE OR FALSE?

A

FALSE

cranial nerves - 12 pairs

spinal nerves - 31 pairs

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5
Q

PNS

which strutures are derived from neural crest cells ?

A

sensory neurons

+

postganglionic autonomic neurons

(cell bodies are found in ganglia)

+

Chromaffi cells

(neural crest cell migrate into the adrenal mdulla to form postganglionic sympathetic neurons)

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6
Q

Neurulation begins in the …

(week)

A

THIRD WEEK

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7
Q

CNS and PNS derived from …

ecto, meso or endoderm?

A

ECTODERM

(neuroectoderm)

notochord overlying ectoderm to form the neural plate (neuroectoderm)

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8
Q

WHEN and HOW neural tube is formed?

A

By the end of the THIRD WEEK

+

neural folds grow over mildline and fuse

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9
Q

Neural crest cells also formed from neuroectoderm

TRUE OR FALSE?

A

TRUE

during the closure of neural folds, neural crest cells are formed

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10
Q

Neural tube closuring

rostral neuropore closes at …

caudal neuropore closes at…

A

ROSTRAL

day 25

CAUDAL

day 27

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11
Q

Failure to close

rostral consequences …

caudal consequences…

+

substances increase ?

A

ROSTRAL

anencephaly (polyhydramios)

CAUDAL

spina bifida

+

ALPHAFETOPROTEIN and AChE are increased

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12
Q

Alphafetoprotein may also be elevated in…

A

Gastroschisis and omphalocele

AFP levels are low in pregnancy of Down syndrome fetus

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13
Q

NEURAL TUBE

the sequence is TRUE or FALSE?

3 primary vesicles –> 5 primary vesicles –> brain and spinal cord

A

TRUE

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14
Q

NEURAL TUBE

alar plate = motor

basal plate = sensory

TRUE OR FALSE?

A

FALSE

alar plate (sensory) and basal plate (motor) are separated by sulcus limitans

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15
Q

NEURAL TUBE

3 primary vesicles?

A

FOREBRAIN

+

MID BRAIN

+

HINDBRAIN

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16
Q

NEURAL TUBE

5 primary vesicles

A

TELENCEPHALON + DIENCEPHALON

(forebrain)

MESENCEPHALON

(midbrain)

METENCEPHALON + MIELENCEPHALON

(hindbrain)

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17
Q

TELENCEPHALON

structures

+

neural canal remnant

A

CEREBRAL HEMISPHERES

+

MOST OF BASAL GANGLIA

+

LATERAL VENTRICLES

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18
Q

DIENCEPHALON

structures

+

neural canal remnant

A

THALAMUS + HYPOTHALAMUS + SUBTHALAMUS + EPITHALAMUS (PINEAL GLAND) + RETINA + OPTIC NERVE

THIRD VENTRICLE

19
Q

MESENCEPHALON

structures

+

neural canal remnant

A

MIDBRAIN

+

CEREBRAL AQUEDUCT

20
Q

METENCEPHALON

structures

+

neural canal remnant

A

PONS and CEREBELLUM

+

FOURTH VENTRICLE

21
Q

MYELENCEPHALON

structures

+

neural canal remnant

A

MEDULLA and SPINAL CORD

+

CENTRAL CANAL

22
Q

CONGENITAL MALFORMATIONS

anecephaly

(cause, main consequence and markers)

A

Failure of anterior neuropore to close

+

brain does not develop

+

incompatible with life

+

AFP and AChE (increase)

23
Q

CONGENITAL MALFORMATIONS

spina bifida occulta

A

Failure of posterior neuropore to close

+

mildest form

+

vertebrae fail to form around spinal cord

+

asymptomatic (tuft oh hair)

+
normal AFP

24
Q

CONGENITAL MALFORMATIONS

spina bifida with meningocele

A

Meninges protude through vertebral defect

+

increase in AFP

25
CONGENITAL MALFORMATIONS spina bifida with meningomyelocele
Meninges + spinal cord protude through vertebral defect + increase in AFP + seen with Arnold-Chiari Type II
26
CONGENITAL MALFORMATIONS spina bifida with myeloschisis
Most severe + spinal cord externally + AChE and AFP increase
27
CONGENITAL MALFORMATIONS Arnold-Chiari type I
cerebellar tonsilis down through foramen magnum + Most commom Mostly Asymptomatic Often association with syringomyelia
28
CONGENITAL MALFORMATIONS Arnold-Chiari type II
cerebellar vermis down through foramen magnum + often symptomatic obstructive hydrocephaly (IV ventricle) often meningomyelocele
29
CONGENITAL MALFORMATIONS Dandy-Walker
Failure to form Luschka and Magendie + dilatation of IV ventricle + agenesis of cerebellar vermis and splenium of the corpus callosum
30
CONGENITAL MALFORMATIONS Holoprosencephaly
Incomplete separation of cerebral hemispheres (one ventricle in telencephalon + Patau (trisomy 13)
31
PNS general organization
32
PNS NEUROTRANSMITTERS/RECEPTORS NT of all preganglionic neurons?
**AChE**
33
PNS NEUROTRANSMITTERS/RECEPTORS receptor of ALL postganglionic neurons?
NN | (neuronal nicotinic receptor)
34
PNS NEUROTRANSMITTERS/RECEPTORS NT of ALL PARASYMPATHETIC POSTGANGLIONIC NEURONS?
AChE
35
PNS NEUROTRANSMITTERS/RECEPTORS receptor of ALL parasympathetic sites in periphery
M (muscarinic receptor) heart, smooth muscle and glands
36
PNS NEUROTRANSMITTERS/RECEPTORS NT of sympathetic postganglionic neurons
1. NE (noripinephrine) 2. Epi (epinephrine) 3. Ach (acetylcholine)
37
PNS NEUROTRANSMITTERS/RECEPTORS receptors of sympathetic sites in periphery
alpha or beta (NE) heart, smooth muscle, glands + muscarinic (ACh) sweat gland, piloerector muscles + alpha or beta (Epi) various organs - transported via blood
38
PNS NEUROTRANSMITTERS/RECEPTORS somatic motor neuron (NT + receptor in periphery)
ACh + Nm (muscle nicotinic receptor) skeletical muscle
39
PANS overview
MOST IMPORTANT THINGS
40
SANS overview
MOST IMPORTANT THINGS
41
SANS Gray Rami
Gray rami are postganglionics that rejoin spinal nerves to go to the body wall
42
PANS Hirschsprung's disease (cause + main consequence)
Missing terminal ganglia in wall of rectum + infant cannot pass mecanium
43
SANS Horner's Syndrome (cause + clinic)
Lesion in the Superior Cervical Ganglion + ipsilateral ptosis, miosis, anhydrosis