Topic # 7 DEVELOPMENT OF THE MUSCULOSKELETAL SYSTEM Flashcards

1
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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2
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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3
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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4
Q

Muscle development requires

A

innervations

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5
Q

by delamination forms mesenchymal cells that elongate to form myoblasts.

A

Splanchnic mesoderm

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6
Q

Cardiac muscle cells are joined together by intercellular
connections called

A

intercalated discs.

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7
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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8
Q

two types of fibers secreted by fibroblasts:

A

collagenous and elastic

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9
Q

originates from paraxial mesoderm, somatic mesoderm or ectomesenchyme

A

Bone

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10
Q

occurs in most bones of the axial skeleton and appendicular skeleton. This occurs by ossification of a cartilage model.

A

Endochondral Bone Development

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11
Q

occurs in bones of calvaria (roof of skull) and face.
Mesenchymal (osteogenic) cells from mesoderm or ectoderm proliferate and aggregate;
become round and enlarged and are now termed osteoblasts.

A

Intramembranous Bone Development

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12
Q

Common Malformations of the Vertebra Alignment Defects

A
  1. Scoliosis
  2. Kyphosis
  3. Lordosis
  4. Torticolis or wry neck
  5. spina bifida
  6. Rachischisis
  7. Spina bifida occulta
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13
Q

lateral deviation of vertebral column.

A

Scoliosis

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14
Q

sagittal deviation of vertebral column in a fixed position.

A

Kyphosis

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15
Q

sagittal deviation of vertebral column in a fixed extended position.

A

Lordosis

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16
Q

abnormal twisting of the cervical vertebral column.

A

Torticolis or wry neck

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17
Q

absence of vertebral arch (failure of vertebral arch to form dorsally
over the vertebral foramen).

A

Spina bifida

18
Q

spina bifida of several adjacent vertebrae.

A

Rachischisis

19
Q

spina bifida covered by skin and subcutis.

A

Spina bifida occulta

20
Q

develops from outward growth of ectomesenchymal tissue located rostral to the cranium and pharynx.

A

face

21
Q

cleft lip caused by failure of fusion of medial nasal and maxillary
processes.

A

Cheiloschisis

22
Q

cleft palate caused by failure of medial palatine processes to fuse.

A

Palatoschisis

23
Q

Primordia of enamel organs
escape to the exterior and develop tooth structures anchored on the parietal bone or
base of the ear.

A

Heterotropic polyodontia

24
Q

loss of a specific part of a limb. It is usually named using the defect
as prefix and the phrase “melia” (melos=limb) or dactyl (Gr. dactylos= digit) as suffix.

A

Limb Reduction

25
Q

inherited; systemic premature
ossification of physes of extremeties.

A

Achondroplasia (dwarfism; Dachshund)

26
Q

complete absence of a limb.

A

amelia

27
Q

absence of a part of a limb.

A

Meroromelia

28
Q

complete absence of limb.

A

Acromelia

29
Q

absence of half or one or more segments of a limb.

A

Hemimelia

30
Q

reduced size of a limb.

A

Micromelia

31
Q

absence of one or more proximal segments, a consequence of
pregnant women taking thalidomide in the late 1950’s.

A

Phocomelia

32
Q

fused digits.

A

Syndactyly

33
Q

shortened or stumpy digits.

A

Brachydactyly

34
Q

absence of one or more digits.

A

Ectrodactyly

35
Q

presence of one or more extra digits. This is common in pig and cat.

A

Limb Duplication

36
Q

one or more extra digits.

A

Polydactyly

37
Q

partial or complete duplication of one limb.

A

Bimelia

38
Q

limb growing from the back of the animal.

A

Notomelia (noto=back)

39
Q

can results from malformed joints, denervation, abnormal muscle tension, or impaired mobility in utero.

A

Arthrogryposis

40
Q

abnormal maturation of the hip joint that results in formation
of a shadow acetabulum and flattened femoral head. Inherited and associated w/ large, muscular breeds of dog. Onset of signs may occur at 3 – 5 months of age.

A

Hip Dysplasia

41
Q

permanent fixation of a joint caused by immobility of the fetus in utero.

A

Ankylosis