DEVELOPMENT OF THE MUSCULOSKELETAL SYSTEM Flashcards

(68 cards)

1
Q

Types of Muscle Cell (Myocyte)

A

Skeletal or striated or voluntary myocyte
Smooth or visceral or involuntary myocyte
Cardiac myocyte

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2
Q

comprises 40 – 45 % of the total body weight.
➢ Long and cylindrical w/ many nuclei located at the periphery of the cell

A

Skeletal or striated or voluntary myocyte

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3
Q

is found in the walls of tubular and visceral
organs.
➢ Spindle-shaped w/ one nucleus located in the middle of the cell

A

Smooth or visceral or involuntary myocyte

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4
Q

comprises the myocardium of the heart.
➢ Branched w/ many nuclei located in the middle of the cell.

A

Cardiac myocyte

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5
Q

Mesodermal cells of myotome of each somite/somitomere separate from dermatome and
sclerotome, and elongate to spindle-shaped that synthesize myosin and actin and
appear striated. Several myoblasts fuse to form multinucleated myotubes

A

myoblasts

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6
Q

The myotubes, with
nuclei that migrate peripherally, present cross striations, and are now called .

A

skeletal myocytes

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7
Q

After birth, the myocytes interact with motor nerves and differentiate into .

A

fast-twitch, slow-twitch
or intermediate myocytes

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8
Q

Muscle development requires

A

innervations

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9
Q

Also, muscles and tendons must be stretched by growing bone) in order to grow proper lengths

A

under
tension(

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10
Q

Each anatomic muscle is
practically allocated a special number of myoblasts that is determined by the time of birth.
Thereafter, muscle cell growth is due solely to

A

cellular hypertrophy.

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11
Q

Epimere becomes

A

epaxial muscles

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12
Q

the hypomere becomes the

A

hypaxial muscles

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13
Q

by delamination forms mesenchymal cells that elongate to
form myoblasts.

A

Splanchnic mesoderm

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14
Q

for smooth muscles of blood vessels

A

Somatic mesoderm

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15
Q

for smooth muscles of the iris.

A

Ectoderm (neural ectoderm of optic cup)

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16
Q

that surrounds the epithelium of a structure or organ for other
smooth muscles.

A

mesenchyme

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17
Q

Cardiac muscle cells are joined together by intercellular
connections called

A

intercalated discs.

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18
Q

Types of Connective Tissues

A
  1. Loose connective tissue - mesenchymal, mucoid, areolar adipose tissue, etc.
  2. Dense connective tissue - tendons, ligaments.
  3. Cartilage
  4. Bone
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19
Q

Mesenchymal cells from mesoderm (somite) or in case of head, from ectoderm (neural
crest) become stellate or spindle-shaped and are now termed .

A

fibroblasts

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20
Q

There are two types of fibers secreted by fibroblasts:

A

collagenous and elastic.

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21
Q

Blood vessels and osteogenic cells invade the calcified cartilage and form the

A

periosteal
bud

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22
Q

The bone trabeculae interconnect to form .

A

cancellous bone

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23
Q

is made possible through the epiphyseal plate, a plate of
cartilage between the diaphysis and epiphysis where the cartilage is continuously
formed and replaced during the growing years of the animal

A

Growth in length of long bone

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24
Q

occurs by deposition of additional layers of bone
substance on the bone surface by osteoblasts in the periosteum of diaphysis and
destruction of bone and cartilage by osteoclasts and chondroclasts, respectively, in
the central portion of diaphysis to create a marrow canal or marrow cavity.

A

Growth in diameter of long bone

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25
Addition of layers of bone matrix reduces the intertrabecular spaces and the cancellous bone in the diaphysis is converted into a
compact bone
26
Osteocytes present cytoplasmic processes that radiate into the matrix through tiny bone channels called
canaliculi
27
The intertrabecular spaces are occupied by blood-forming cells (red bone marrow) and are also called
marrow spaces
28
Common Malformations of the Vertebra Alignment Defects
Scoliosis Kyphosis Lordosis Torticolis or wry neck Spina bifida Rachischisis Spina bifida occulta
29
- lateral deviation of vertebral column
Scoliosis
30
- sagittal deviation of vertebral column in a fixed position
Kyphosis
31
- sagittal deviation of vertebral column in a fixed extended position
Lordosis
32
- abnormal twisting of the cervical vertebral column
Torticolis or wry neck
33
- absence of vertebral arch (failure of vertebral arch to form dorsally over the vertebral foramen).
Spina bifida
34
– spina bifida of several adjacent vertebrae
Rachischisis
35
- spina bifida covered by skin and subcutis
Spina bifida occulta
36
- does not ossify
Nasal capsule
37
- ethmoid and bone around the pituitary gland
Prechordal cartilage
38
- base of occipital bone
Parachordal cartilage
39
- temporal bone
Otic capsule
40
develops from outward growth of ectomesenchymal tissue located rostral to the cranium and pharynx.
Face
41
Malformations of the Face
Cheiloschisis Palatoschisis Branchial cyst ( Heterotropic polyodontia -
42
- cleft lip caused by failure of fusion of medial nasal and maxillary processes.
Cheiloschisis
43
- cleft palate caused by failure of medial palatine processes to fuse
Palatoschisis
44
(no opening)
Branchial cyst
45
(opening to exterior)
branchial sinus
46
(openings to interior and exterior).
branchial fistula
47
- (dentigerous cyst, ‘ear teeth’). Primordia of enamel organs escape to the exterior and develop tooth structures anchored on the parietal bone or base of the ear.
Heterotropic polyodontia
48
Types of Limb Malformations
Limb Reduction Limb Duplication Limb and Joint Deformities
49
Type of Limb Reduction
Achondroplasia (dwarfism; Dachshund) Amelia Meroromelia Acromelia Hemimelia Micromelia Phocomelia Syndactyly Brachydactyly Ectrodactyly
50
inherited; systemic premature ossification of physes of extremeties
Achondroplasia (dwarfism; Dachshund) -
51
- complete absence of a limb.
Amelia
52
- absence of a part of a limb.
Meroromelia
53
– complete absence of limb.
Acromelia
54
– absence of half or one or more segments of a limb
Hemimelia
55
- reduced size of a limb.
Micromelia
56
- absence of one or more proximal segments, a consequence of pregnant women taking thalidomide in the late 1950’s
Phocomelia
57
- fused digits.
Syndactyly
58
- shortened or stumpy digits
Brachydactyly
59
- absence of one or more digits
Ectrodactyly
60
Type of Limb Duplication
Polydactyly Bimelia Notomelia (noto=back
61
- presence of one or more extra digits. This is common in pig and cat
Limb Duplication
62
- one or more extra digits
Polydactyly
63
- partial or complete duplication of one limb
Bimelia
64
- limb growing from the back of the animal.
Notomelia (noto=back)
65
Type of Limb and Joint Deformities
Arthrogryposis Hip Dysplasia Ankylosis
66
- crooked limb. Gr. gryposis=crooked) - can results from malformed joints, denervation, abnormal muscle tension, or impaired mobility in utero.
Arthrogryposis
67
- abnormal maturation of the hip joint that results in formation of a shadow acetabulum and flattened femoral head.
Hip Dysplasia
68
- permanent fixation of a joint caused by immobility of the fetus in utero.
Ankylosis