Exam 3 Chapter 9 Flashcards

1
Q

The dividing somite is made up of mesodermal cells, these give rise to:

A

Mesenchyme

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2
Q

The skeletal system is derived from ______. & mesenchyme of the head & limbs

A

Sclerotomes

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3
Q

Condensation of the mesenchyme gives rise to the bone models:

A

Cartilage: Endochondral or intercartilagenous
Membrane: Intramembranous

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4
Q

Neurocranium: Develops from what surrounding the brain?

A

Mesenchyme

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5
Q

What are the 2 types of neurocranium development?

A
  • Neurochondrocranium

- Neuromembranocranium

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6
Q

Neurochondrocranium builds what?

A

cartilage base for growing brain

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7
Q

Neuromembranocranuim forms what?

A

the sides & the roof of the neurocranium.

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8
Q

Anterior fontanelle - closes end of:

A

2nd yr.

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9
Q

Posterior & anterolateral fontaelle- closes:

A

2-3 months

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10
Q

Posterolateral closes:

A

End of the 1st year

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11
Q
  • Develops from mesenchyme of the sclerotome
  • Caudal portion densely packed
  • Cranial part loosely packed
  • Cranial portion moves up the caudal portion
  • These portions fuse to make the vertebra
  • This action makes room for the vessels & muscles
A

Vertebra Development

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12
Q
  • Doesn’t fuse untio 3rd month after birth
A

Spinous process

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13
Q

5 Ossification centers @ puberty

A
  • 1 @ tip of spinous process
  • 1 @ each tip of transverse process
  • 2 on the rim of the epiphyseal center
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14
Q
  • Intramembranous

- Ossifies before other bones in the body

A

Clavicle development

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15
Q
  • Small stature
  • Craniofacial- large face & head
  • Skeletal- short tubular bones
  • Hyper lordosis in lumbars
  • Etiology: autosomal dominate
A

Achondroplasia syndrome - slow growth of cartilage

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16
Q
  • Lipids accumulate in the mesenchyme & nervous system
  • Grow is stunted & nervous system is compromised - Lower IQ
  • Hunter’s & Hurler’s Syndrome
A

Mucopolysaccaridosis

17
Q

What types of Spina Bifida are there?

A

Occulta- Can’t see on the outside

Cystica - with a cyst

18
Q

Occulta (Spina bifida)

A

Limited to the vertrbra

usually spinous process

19
Q

Cystica (spina bifida)

A

Meninges only - meningocoele

Meninges & spinal cord- Meningomyelocoele

20
Q
  • Abnormal curvature of the spine
  • Number of vertebra varies
  • Morphological variation- did not develop correctly
A

Congenital Scoliosis

21
Q

Premature closure of the sutures of the skull

A

Craniostenosis

22
Q

Oxycephaly

A

All sutures are closed - symmetrical

23
Q

Plagiocephaly

A

Sutures close asymmetrical

24
Q

Scaphocephaly

A

Sagittal sutures close prematurely - long narrow cranium

25
Acrocephaly
Coronal sutures close - shorten wide cranium
26
Absence of limbs
Amelia
27
Absence or reduction of proximal limb
Phocomelia
28
Absence or reduction of distal part of limb
Meromelia
29
Fusion of lower limb
Sympodia (mermaid syndrome)
30
Duplication of distal part of limbs- Can be addition of hands & feet
Dichiria
31
Presence of extra digits
Polydactyly
32
Fusion of digits or digit
Syndactyly