Development of Bones and Muscles- Fields Flashcards

1
Q

somitomeres develop into what along spine below the head

A

somites

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2
Q

collection of cells that are derived from paraxial mesoderm

A

somitomeres

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3
Q

somite forms into 3 regions:

A

sclerotome (bone)
dermatome (dermatomes of dorsal region)
myotome (muscle)

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4
Q

part of axial skeleton formed from intramembranous ossification

A

facial bones and most bones of skull

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5
Q

part of axial skeleton that develops from endochondral ossification

A

everything else but facial bones and most bones of skull

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6
Q

genes essential for proper spatial development of vertebral column bones

A

HOX genes

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7
Q

taken during early development will disrupt HOX genes and cause cranial shift

A

vitamin A (retinoic acid)

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8
Q

short neck with a reduced number of cervical vertebrae (cranial shift) from disrupted HOX genes

A

Klippel-Feil Syndrome

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9
Q

taking vitamin A (retinoic acid) later during development causes what shift

A

caudal shift

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10
Q

____ develop with the vertebrae as a single bone and will later separate

A

ribs

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11
Q

axial skeleton bone formed from somatic lateral plate mesoderm

A

sternum

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12
Q

starts out as 2 different plates but will fuse if developed normally

A

sternum

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13
Q

vertebral arch doesn’t fuse, exposing spinal cord

A

dysraphism

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14
Q

failure of proper fusion of sternal bands

A

split sternum

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15
Q

failure of proper fusion of sternal bands

A

Bifid Xiphoid process

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16
Q

failure of proper fusion of sternal bands

A

sternal and xiphoid foramen

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17
Q

abnormal sternum formation

A

pes carinatum

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18
Q

abnormal sternum formation

A

pes excavatum

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19
Q

formed from somatic lateral plate mesoderm

A

appendicular skeleton

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20
Q

only appendicular skeleton bone formed from intramembranous ossification

A

clavicle

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21
Q

formed from scleratome of paraxial mesoderm

A

axial skeleton

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22
Q

absense of 1 or both clavicles

A

cleidocranial dysplasia

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23
Q

defects of the limb

A

melia

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24
Q

defects of the digits

25
2 main reasons for congenital anomalies of extremities
environment and genetics
26
Wnt (used for dorsal muscles)
27
limb buds form by ____ week and limbs pointed out and thumbs and big toes pointed up
4th
28
responsible for proximal/distal and cranial/caudal pattern of bones
HOX genes
29
develops from ectoderm and is responsible for proximal/distal pattern of bones
Apical Ectodermal Ridge (AER)
30
order of AER and limb skeletal formation
FGF-8 stimulates SHH to produce SHH signaling molecule and HOX (high amount of SHH proximal)
31
growth center responsible for cranial/caudal pattern of bones
zone of polarizing activity (ZPA)
32
ZPA and limb skeletal formation
FGF-8 stimulates SHH to produce SHH + HOX; higher amount of SHH at caudal region)
33
upper extremities dependent on this gene
Tbx-5
34
lower extremities dependent on this gene
Tbx-4
35
Tbx-5 mutation that deals with hand and arm deformities
Holt Orman Syndrome (HOS)
36
Tbx-4 mutation that deals with lower limb dysplasia
small patella syndrome
37
overexpression of SHH OR can be caused by excess BMP
polydactyly
38
underexpression of SHH
Hemimelia
39
underexpression of SHH (shortened upper limbs and missing bone)
Meromelia
40
protein responsible for apoptosis between digits
bone morphogenic protein (BMP)
41
apoptotic failure due to mutation of FGF or BMP
syndactyly
42
over-expression of BMP
lobster claw
43
happens around week 8 and thumb ends up lateral and big toe ends up medial
limb rotation
44
signaling molecules that stimulate proper digital formation
FGF and BMP
45
interact with HOX genes for proper formation of limb bones and joints
T-box genes
46
a form of dwarfism caused by a deficiency of thyroid hormone
Cretinism
47
large jaw, hands, feet, due to hyperpituitarism
Acromegaly
48
sirenomelia (mermaid syndrome)
49
signaling molecules used in skeletal muscle development
Wnt, BMP, Engrailed (En-1)
50
signaling molecules in skeletal muscle formation stimulate what that helps mesenchymal cell transformation to myoblast
Pax-3
51
signaling molecule for dorsal signaling of trunk muscle development that stimulates Pax-3
Wnt
52
signaling molecule for ventral signaling of trunk muscle development that stimulates Pax-3
BMP-4
53
mutation in BMP causes this; failure of ventral abdominal musculature to form
prune belly
54
signaling molecule for limb muscle development that deals with dorsal m. signaling; stimulates Pax-3
Wnt-7
55
signaling molecule used for limb muscle development that deals with ventral m. signaling; stimulates Pax-3
En-1 (engrailed-1)
56
myoblasts from myotome migrate where to form limbs
limb buds
57
responsible for nerve migration (GSE, GSA)
connective tissue
58
overexpression of engrailed (ventral muscle)