Final Exam Flashcards

(123 cards)

1
Q

The dividing somite is made up of mesodermal cells that give rise to the

A

Mesenchyme

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2
Q

The skeletal system is derived from the

A

Sclerotomes, and mesenchyme of the head, and limbs.

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3
Q

Condensation of the mesenchyme gives rise to these two bone models

A

Cartilage - Endochondral

Membrane- Intermembranous

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4
Q

In this model, the mesenchyme condenses and makes chondroblasts (cells that make cartilage).

A

Cartilage model

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5
Q

The chondroblasts in the cells kick start this process in which cartilage starts forming a template

A

Chondrification

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6
Q

Once the cartilage template in the cartilage model is done, the fibers and the matrix within it start forming this tissue

A

Pre-osseus tissue

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7
Q

Once the preosseus tissue is formed, we find ourselves in the cartilage stage of bone development where in the _____ grows rapidly

A

Fetus

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8
Q

In this model of bone development the mesenchyme condenses and becomes vascular points that develop osteoblasts

A

Membrane model

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9
Q

In the membrane model, these cells begin to deposit osteoid tissues that will later become ossification centers of the respectives bones

A

Osteoblasts

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10
Q

In the membrane model, this structure makes spicules become lamella forming around blood vessels or osteons

A

Bone matrix

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11
Q

Both cartilage and membrane models become bone tissue by depositing ________ in the _______ tissue

A

Calcium salts; Osteoid tissue

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12
Q

The depositing of calcium salts causes the osteoblasts to become trapped and thus become

A

Osteocytes

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13
Q

This structure builds a cartilage base for the growing brain as well as the Nasal base, orbital base, hypophyseal or pituitary base, otic or ear base, and the occipital base

A

Neurochondocranium

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14
Q

This membrane bone develops the parietals, frontal, vomer, nasal and lacrimal areas

A

Neuromembranocranium

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15
Q

The fontanelles and sutures of the cranium formed by the neuromembranocranium have different ossification times. (They close at different times)

The anterior fontanelle closes at ____

The posterior and anterolateral fontanelle closes in ______

The posterolateral closes at _____

A

The end of the 2nd year, 2-3 months, end of 1st year

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16
Q

This bone structure makes up the face and the neck area, It is made through the cartilage model of growth and comes forth from the visceral arches

A

Splanchnochondrocranium

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17
Q

These bones develop from the mesenchyme of the sclerotome and have a densely packed caudal portion and loosely packed cranial part.

A

Vertebra

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18
Q

In order for the vertebra to fuse together the cranial portion must __________ making room for the vessels and the muscles to develp

A

move up

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19
Q

This shows up more lighter than the vertebra and does not fuse until the 3rd month after birth

A

Spinous process

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20
Q

The vertebra has ____ ossification centers at puberty

A

5

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21
Q

Where are the ossification centers for the vertebra located

A

1 at tip of spinous process

one at each tip of the transverse process

two on the rim of the epiphyseal center

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22
Q

The mesenchymal bands start and fuses to the ribs these bands then fuse together to give rise to this specific upper extremity bone

A

Sternum

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23
Q

This bone undergoes intramembranous development and ossifies before other bones in the body

A

Clavicle

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24
Q

A consequence of slow cartilage growth.

Patients who have this malformation exhibit

Small stature, large face and head, short tubular bones, and hyper lordosis in lumbars

A

Achondroplasia and hypochondroplasia, which has less severe symptoms

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25
There are two types of spina bifida. They are
Occult - not visible from outside Cystica - forms a cyst
26
When the cyst is only in the meninges it is known as
Meningocoele
27
When the cyst is found both in the spinal cord and the meninges it is known as
Meningomyelocoele
28
A malformation where there is an abnormal curvature of the spine. The number of vertebra vary It is due the spine having a morphological variation or that it did not develop properly
Congenital Scoliosis
29
A type of craniostenosis where all sutures are closed and it is symmetrical
Oxycephaly
30
A type of carniostenosis with asymmetrical closure of sutures
Plagiocephaly
31
A type of craniostenosis where the sagittal sutures close prematurely; Long narrow cranium
Scaphocephaly
32
A type of craniostenosis in which the coronal sutures close prematurely and has a shorter wide cranium
acrocephaly
33
A congenital malformation in which limbs are absent
Amelia
34
Congenital malformation in which there is absence or reduction of the proximal limb
Phocomelia
35
Absence or reduction of the distal part of the limb
Meromelia
36
Fusion of the lower limb; also known as mermaid syndrome
Sympodia
37
A duplication of distal part of limbs, this malformation in which there can be an addition of hands and feet
dichiria
38
The presence of extra digits, this malformation is known as
polydactyly
39
The malformation in which digits are fused
Syndactyly
40
The muscle system develops from this layer
Mesoderm
41
The muscle system starts out with two divisions. They are the :
Epimere/Epiaxial and Hypomere/Hypaxial
42
The small dorsal division of the muscle system which forms extensor muscles of the vertebral column. The innervation is provided by the dorsal primary rami
Epimere/epiaxial
43
This is the large ventral division of the muscle system. This division forms muscles of limbs and body wall. The innervation to this division is due to the ventral primary rami
Hypomere/hypaxial
44
This myotome undergoes migration in development
Latissimus dorsi
45
This myotome undergoes fusion in development
Rectus abdominis
46
This myotome undergoes degeneration in development to form a ligament
Tensor fascia lata with the fascia lata
47
The trigeminal nerve innervates this arch
1st Branchial Arch
48
The facial nerve innervates this arch
2nd branchial arch
49
the glossopharyngeal nerve innervates this arch
3 branchial arch
50
the vagus and hypoglossal innervate these arches
4th and 6th branchial arch
51
In this malformation, the muscles are bilaterally absent or underdeveloped
Prune Belly
52
This is a malformation which affects the SCM. The SCM is injured DURING development and becomes fibrous
congenital torticollis
53
The urinary system develops from this layer
Intermediate mesoderm
54
The development of the urinary system begins with the development of the urogenital ridge which then becomes the nephrogenic mass. The cells that are formed from the ridge and break up into segments are called
Nephrotomes
55
There are three kidneys that formed during development. These are known as:
Pronephrol, mesonephrol, and mesonephrol
56
This kidney is known as the head Kidney, it has open tubule which drain into the coelom. It is also found on the 7th-10 somite level
Pronephrol
57
This kidney functions briefly and is found on the 10-26th somite level. It has closed tubules which connect to the glomerulus. These tubules are retained to in the male for the reproductive system
Mesonephrol
58
This kidney is found on the 26th to the 28th somite level. Has around 2 million closed tubules. Associated to renal pelvis
Metanephrol
59
In bladder developmente the mesodermal mass divides the cloacal septum into two divisions. These are the :
Dorsal which forms the rectum Ventral which forms the urinary bladder
60
This structure is the neck that is continuous with the cloaca and becomes ligamentous when the bladder develops. In the fetus in is known as the uracus. In the adult it is known as the median umbilical ligament
Allantois
61
This malformation is found in infants. Most of the infants suffer early death and have spongy kidneys which are symmetrically enlarged
Type 1 Congenital Cystic Kidney
62
This malformation is manifested in adults and present before birth. Symptoms include low back pain and kidney infections
type 5 congenital cystic kidneys
63
These tumors have many types of names and derive from the mesoderm. They also have a high growth rate.
Wilm's tumors
64
This system has its origins in the intermediate mesoderm. Sex or germ cells from the yolk sac travel to the genital ridge to become primary sex cords and then develop undifferentiated gonads
The reproductive system
65
The hormone associated with the differentiation of gonads is known as
TDF
66
In the case of development of the reproductive system the male cortex regresses and the medulla develops. In females the cortex _____ and the medulla______
develops ; regresses
67
Spermatoblasts are formed from the
Testes cords
68
The female cords break up into these primordial follicles
Ooblasts and follicular cells
69
The mesoneprhic ducts in the male reproductive system form the
epididymis and ductus deferens
70
The paramesonephric ducts are y shaped and develop the
uterus and the vagina
71
Ovarian hypoplasia that is bilateral. Infertility if hypoplasia is unilateral they are fertile this congenital malformation is known as
Turners syndrome
72
In this congenital malformation the person appears to be a female. They have shallow vaginas and presence of testes in abdominal area There body cells dont respond to testosterone and they are chromatin negative
Androgen insensitivity
73
A female has masculinization of her genitals and has excessive androgen production. This malformation is known as
Androgenital syndrome
74
Blood cell development happens because of this layer
Splanchnic mesoderm
75
These vessels return blood from the embryonic yolk sac
Vitelline vessels
76
These vessel sbring blood from the placenta
umbilical veins
77
These vessels return blood from the embryonic body
Cardinal veins
78
Two endothelial tubes fuse to form a single tube. Later on, the ventricles of this organ are formed and grow much faster than do the atrium. The ventricles then push the atrium portion of the organ up to the upper portion. This is a rough description of the development of the
Heart
79
The heart divides into ___ chambers
4
80
In the atrium we have the 1st wall or the _______.
Septum primum
81
The 1st opening in the septum primum is known as the
Ostium primum
82
the secondary opening in the 1st wall is known as the
Ostium secundum
83
The second wall of the atrial system is known as the
Septum secundum
84
opening in septum secundum to communicate with ostium secundum also an interatrial shunt during development atria communicates with each other.
Oval foramen
85
The contraction of the heart begins in the ___ day
22nd
86
Shunts in the fetal pulmonary trunk that divert blood back to the aorta
Ductus arteriosus
87
shunt in the fetal heart that causes oxygenated blood to bypass the fetus developing liver to reach the vena cava
Ductus venosus
88
The great vessel is divided by spiral growth into these two other vessels
ascending aorta and the pulmonary trunk
89
Absence of the heart
Acardia
90
Heart is located outside of the body
Ectopic cordis
91
Heart is located in the right hemithorax
dextra cardia
92
Dextra cardia with organs mirror image
situs inversus
93
Malformation in which there can be a large hole in the atrium with a loud systolic murmur. Causes cyanosis
Arterial septal defect
94
This malformation has a hole in the ventricle system of the heart but causes no cyanosis
Ventricular septal defect
95
An agent that produces a congenital malformation is known as a
Teratogen
96
In etiology, Objective evidence of a diseases is known as a
Sign
97
In etiology, the subjective evidence of a disease is known as
symptom
98
In etiology, a set of symptoms and signs which occur together
Syndrome
99
The study and cause of disease is known as
Etiology
100
The nervous systems form between the ____ and ____ weeks
3rd and 7th
101
The cardiac systems from between the ____ and ____ weeks
4th and 6th
102
The ears form betwewn the ___ and _____ weeks
4th and 8th
103
The eyes form between the ____ and ____ weeks
4th and 8th weeks
104
the limbs form between the _____ and _____ weeks
4th and 7th weeks
105
Chromosome disorder which could result from abnormal cell division that can happen in meiosis 1 and/or 2 This abnormal division may lead to an abnormal number of chromosomes this is known as
Nondisjunction of chromosomes
106
Also known as Down's syndrome. Patients have 47 (21) chromosomes They usually exhibit hyperflexed joints, microcephaly, simian crease in the palmar surface of the hand, and have intellectual disability.
Trisomy 21
107
Also known as edwards syndrome. Patients have 47(18) of chromosomes Failure to thrive is prevalent, have rocker bottom feet and flexion deformation of fingers
Trisomy 18
108
A trisomy of this sex chromosome leads to scanty menses and many of the patient that exhibit it are fertile. The cardiac and facial features are normal and the patient may appear normal
Trisomy of X
109
Patient has 47 chromosomes Sex chromosomes : XXY They exhibit long legs in proportion to their trunk (abdomen) Exhibit cryptorchism and are usually chromatin positive
Klinefelters syndrome
110
As opposed to trisomy, this syndrome is known to be a monosomy of a sex chromosome. Patient has 45 X0 or 45 X chromosomes Exhibit short stature, webbed neck, skeletal deformation, some are fertile however they posses a lack of breast development infantile external genitalia and are chromatin negative
Turners syndrome
111
Cat eye syndrome : Patient exhibits 46 chromosomes, anal atresia, and inferior coloboma (elongation of the pupil) This type of chromosomal anomaly is known as
Addition of part chromosome
112
When there is deletion of a part chromosome the infant exhibits high pitched crying, hypotonia and simian crease. this syndrome is known as
Cri-du-chat
113
This pathogen has the following effects on the mother: chicken pox and shingles On the fetus: viremia
Varicella zoster
114
This pathogen has the following maternal effects: vulvo vaginitis on the fetus: fetal death, skin eruptions, calcification on the brain
Herpes
115
This pathogen causes german measles on the mother and deafness or cataracts in the fetus/newborn
rubella
116
this pathogen causes genital tract infection and formation of scar tissue in the uterine tubes of the mother on the fetus it could cause infection of the conjunctiva
Gonorrhea
117
This protozoa causes toxoplasmosis on the mother which could be asymptomatic On the fetus, could cause abortion or mental retardation on the newborn Could also cause calcification of the brain
Toxoplasma gondii
118
Drugs for which studies have not shown risk to the fetus
Category A drugs
119
Drugs with now human studies but animal studies have shown an effect on the fetus
Category B
120
Drug studies are inadequate in both humans and animals to show an effect to the fetus
Category C
121
Drugs that will cause harm to the fetus but benefits the mother
Category D
122
Drugs that dont cause any harm to the mother but cause damage to the fetus
Category X
123
These are the _____ of radiation: production of free radicals breakage of chemical bonds and production of new ones between macromolecules Damage of DNA and RNA
Mechanisms of damage