7 Flashcards

(62 cards)

1
Q

from mesoderm or ectoderm proliferate and
aggregate;

A

Mesenchymeal (chondrogenic) cells

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2
Q

become round and enlarged and are now termed

A

Chondroblasts

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3
Q

secrete amorphous ground substance

A

Chondroblasts

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4
Q

to form the cartilage matreix

A

collagen
fibers

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5
Q

Originates from paraxial mesoderm, somatic mesoderm or ectomesenchyme

A

Bone

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6
Q

occurs in most bones of the axial skeleton and
appendicular skeleton.

A

Endochondral bone development

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7
Q

Cartilage model

A

ossification

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8
Q

chondroblasts secrete matrix to produce a cartilage model of the
future bone; the model is surrounded by

A

perichondrium

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9
Q

Addition of layers of bone matrix reduces the intertrabecular spaces and the cancellous
bone in the diaphysis is converted into a

A

Compact bone

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10
Q

creating
a smooth surface lubricated by

A

synovial fluid in the joint cavity

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11
Q

Osteoblasts also secrete calcium to the osteoid to
form

A

bone trabecula

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12
Q

me non-secretory and are now termed osteocytes.
Osteocytes present cytoplasmic processes that radiate into the matrix through tiny bone
channels called

A

Canaliculi

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13
Q

A bone with large intertrabecular spaces is classified as

A

cancellous or spongy bone

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14
Q

The intertrabecular spaces are occupied by blood-forming cells
(red bone marrow) and are also called

A

marrow spaces or marrow cavities

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15
Q

Joints must move during in utero and postnatal
development to prevent

A

ankylosis

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16
Q

Sclerotomal mesenchymal cells lateral to the thoracic vertebrae differentiates into

A

cartilaginous ribs

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17
Q

which are eventually destroyed and replaced by

A

bony ribs ( cancellous bone)

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18
Q

The sternum develops differently, from 2 longitudinal aggregations of somatic
mesaenchyme (somatic mesoderm) called

A

sternal bars

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19
Q

. The two (2) sterna bars fuse in the
ventral midline and become segmented to form

A

eight (8) sternebrae

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20
Q

lateral deviation of vertebral column

A

Scoliosis

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21
Q

sagittal deviation of vertebral column in a fixed position

A

Kyphosis

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22
Q

sagittal deviation of vertebral column in a fixed extended position.

A

Lordosis

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23
Q

abnormal twisting of the cervical vertebral column

A

Torticolis or wry neck

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24
Q

absence of vertebral arch

A

Spina bifida

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25
spina bifida of several adjacent vertebrae.
Rachischisis
26
spina bifida covered by skin and subcutis.
Spina bifida occulta
27
The cartilaginous structures fuse and ossify to form the bones of the
floor of the skull.
28
does not ossify
Nasal capsule
29
ethmoid and bone around the pituitary gland
Prechordal cartilage
30
base of occipital
Parachordal cartilage
31
temporal bone
Otic capsule
32
Intramembranous bones articulate by means of fibrous joints called
Sutures
33
Widened suture areas, at the corners of growing bones are called
Fontanels
34
develops from outward growth of ectomesenchymal tissue located rostral to the cranium and pharynx.
Face
35
Ectomesenchymal cells around prosencephalon completely envelop the prosencephalon to form the
frontonasal prominence
36
located between VC1 and VC2, becomes the external auditory meatus.
VC1 or hyomandibular cleft
37
are overshadowed by the expanding hyoid arch and fuse to form a cervical sinus that later disappears w/out a trace.
VC2 to VC4
38
cleft lip caused by failure of fusion of medial nasal and maxillary processes.
Cheiloschisis
39
cleft palate caused by failure of medial palatine processes to fuse
Palatoschisis
40
no opening
Branchial cyst
41
opening to exterior
branchial sinus
42
Openings to interior and exterior
branchial fistula
43
Primordia of enamel organs escape to the exterior and develop tooth structures anchored on the parietal bone or base of the ear.
Heterotropic polyodontia
44
loss of a specific part of a limb
Limb reduction
45
presence of one or more extra digits.
Limb Duplication
46
inherited; systemic premature ossification of physes of extremeties.
Achondroplasia (dwarfism; Dachshund)
47
complete absence of a limb.
Amelia
48
absence of a part of a limb.
Meroromelia
49
complete absence of limb.
Acromelia
50
Absence of half or one or more segments of a limb
Hemimelia
51
reduced size of a limb.
Micromelia
52
absence of one or more proximal segments, a consequence of pregnant women taking thalidomide in the late 1950’s.
Phocomelia
53
fused digits
Syndactyly
54
shortened or stumpy digits.
Brachydactyly
55
absence of one or more digits.
Ectrodactyly
56
presence of one or more extra digits. This is common in pig and cat.
Limb Duplication
57
one or more extra digits
Polydactyly
58
partial or complete duplication of one limb
Bimelia
59
limb growing from the back of the animal
Notomelia (noto=back)
60
crooked limb. Gr. gryposis=crooked) - can results from malformed joints, denervation, abnormal muscle tension, or impaired mobility in utero.
Arthrogryposis
61
abnormal maturation of the hip joint that results in formation of a shadow acetabulum and flattened femoral head.
Hip Dysplasia
62
permanent fixation of a joint caused by immobility of the fetus in utero.
Ankylosis