Week 3 Embryonic Dev. - Ach Flashcards

1
Q

What are the functions of a notochord?

A

define axes
mechanical role in folding process
Induces signaling for the neural tube

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2
Q

What does the neural tube induce?

A

formation of the somites

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3
Q

What is mesenchyme?

A

embryonic connective tissue

multipotent

derived from mesoderm and neural crest

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4
Q

What week do limb buds appear??

A

WEEK FOUR!

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5
Q

Why is week 4 a critical period?

A

Neural tube begins to close
Appearance of somites
Limb buds appear
Organ systems start developing

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6
Q

How are somites formed? How many pairs are formed?

A

Somitomeres become compacted and bound by epithelium to become somites.

42-44 paris are formed

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7
Q

Which pairs remain somitomeres and do not compact into somites?

A

Pairs 1- 7

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8
Q

What are somitomeres?

A

paired blocks of loose mesoderm derived from paraxial mesoderm. They form segmentally along each side of neural tube at the end of the 3rd week

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9
Q

What happens in intramembranous ossification?

A

Mesenchymal cells differentiate directly into osteoblasts

EX: flat skull bones

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10
Q

What happens in endochondral ossifications?

A
  • long bone formation
  • Mesenchymal cells transforms into chondroblasts

-chondroblasts hyaline cartilanginous model

  • deposition of ca+
  • Osteoblasts in diaphysis form primary ossification center
  • osteoblast replace cartilage with bone
  • Growth plate (epiphyseal) continues to lay down hyaline cartilage, lengths bone from diaphysis toward epiphysis
  • Secondary ossification centers are in epiphysis (most form postnatally). Growth toward daiphysis
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11
Q

How is bone age determined?

A

presence/absence of ossification centers and status of growth plate

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12
Q

Achondroplasia

A

can’t covert all the cartilage into bone

most common form of dwarism (limbs short)

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13
Q

Acromegaly

A

excess growth hormone secretion after closure of growth plates. INCORRECT PORPORTIONS. Big head, feet, and hands

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14
Q

Gigantism

A

excess growth hormone before growth plase closure. NORMAL PORPORTIONS. Big overall

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15
Q

Marfan Syndrome

A

Mutations in fibrillin-1
Affects connective tissue
Results in long limb, cardio and lung problems (Abe lincoln)

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16
Q

Osteogenesis imperfecta

A

Type 1 collagen gene
Extreme bone fragility
Sponateous fractures

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17
Q

Congenital Hip DYsplasia/ Dislocation

A

Incomplete formation of acetabulum (femurs can’t stay in place). Legs help at different positions, less movement, uneven leg length

18
Q

Where do smooth muscles of the gut and respiratory come from?

A

Originates from splanchnic mesoderm of the lateral plate

19
Q

Explain resegmentation of the vertebral column during development

A
  • sclerotome cells surround notocord.
  • Each segment is divided by an intersclerotomic fissure (von Ebner’s)
  • this is where the spinal nerves will go through
  • then each vertebra is formed by the dense part of one somite and the loose of another
20
Q

Describe formation of the intervertebral discs

A

The von ebners fissures become the discs.
Nucleus pulposis is derived from the notochrod.
The annulus fibrosis derived from the sclerotome

21
Q

Spinda bifida

A

failure of the neural tube to close. (occulta, meningocele, meningomyelocele)

22
Q

Spinda bifida occulta

A

least severe

marked by tuft of hair

23
Q

Spina bifida meningocele

A

meninges protrude through defect in spindal cord or skull

cyst, but cord is not in cyst

24
Q

Spinda bifida meningomyelocele

A

meninges and spinal cord protrude through defect. Most severe

25
Congenital dermal sinus
neural ectoderm fails to completely separate from the surface ectoderm. Spinal cord may be tethered
26
hemivertebra
caused by failure of ossification center on one side of vertebral body (can cause congenital scoliosis)
27
Congenital brevicollis
shortened neck due to non-segmentation of cerical vertebrae. Limited movement of neck, low hairline.
28
Pectus excavatum
excess cartilage in sternum. Repairable. Concave chest
29
Thoracic outlet syndrome
C7 forms rudimentary rib that can compress neurovascular structures
30
What do myoblasts in epimere form? What innervates them?
deep muscles of the back. Erector spinae -innervated by the dorsal primary rami
31
What do myoblasts in the hypomere from? what innervated them?
the trunk wall. | -ventral primary rami
32
Poland syndrome
underdevelopment of absence of pectoralis muscles
33
Prune belly syndrome
poor development of abdominal muscle wall causing skin to wrinkle
34
Congenital torticollis
spasm of shortening of one side of sternocleidomastoid muscle. Head twisted to one side.
35
apical ectodermal ridge (AER)
growth proximal to distal cells further from AER differentiate -AER also induced apoptosis to get rid of webs between fingers
36
Zone of polarizing activity (ZPA)
- responds to FGFs from AER | - determines anterior vs. posterior (thumb vs. little finger)
37
Amelia
absence or malformation of one or more limbs
38
Meromelia or Phocomelia
partial absence of one or more limbs. Reduction in long bone length
39
Polydactyly
duplication of digits | most common is little finger
40
Syndactyly
failure of apoptosis resluts in webbed finers and or/toes. Can be inherited or develop in isolation.
41
Clubfoot
unusal positioning of foot