Test 4 - GI, Neuro, immunology, endocrine Flashcards

1
Q

When does the Gi tract start to develop? and it progresses from Cranial-to-caudal

A

4th week

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2
Q

By the 4th week, what is present?

A

Intestine and liver

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3
Q

By what week does the urorectal septum fuse with the cloacal membrane which separates the rectum from the bladder

A

Week 7

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4
Q

What anchors the liver to the anterior abdominal wall?

A

falciform ligament

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5
Q

When is the diaphragm complete and the intestinal vili developes?

A

Week 8

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6
Q

When do the intestines re-enter the abdominal cavity?

A

Week 9-10

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7
Q

When do the pancreatic islet cells appear?

A

Week 12

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8
Q

When do the nerve cells start to innervate the bowel - neural crest cell colonize gut? This is where hirschsprung’s disease may form.

A

Week 13

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9
Q

When is meconium present and swallowing present?

A

Week 16

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10
Q

What are four major functions of the Enteric Nervous System?

A

Motility
Microcirculation
Secretions
Immune Respones

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11
Q

When is the sucking/swallowing coordinated?

A

34-36weeks

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12
Q

What is when the ventral bud of the pancreas encircles the duodenum which causes occlusion?

A

Annular Pancreas

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13
Q

At what week can esophageal atresia or stenosis form d/t failure of the lumen to recanalize?

A

Week 8

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14
Q

By what week does the midgut herniate into the umbilical cord and when does it return to abd cavity?

A

6 weeks - 10 weeks

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15
Q

When does omphalocele and gastroschisis usually appear?

A

Week 8-11weeks

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16
Q

When the rectum ends above the puborectails muscle?

A

anorectal agenesis

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17
Q

When the rectum ends below the puborectails muscle?

A

anal agenesis

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18
Q

The failure of the neural crest cells to migrate to the distal colon (lack of ganglion cells in the sigmoid colon and rectum)

A

Hirschsprung’s disease

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19
Q

What are infants more at a risk for if they have Hirschprung’s disease?

A

Hearing loss and decreased peripheral nerve function?

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20
Q

What is when the colon, urinary, and genital systems all empty via one common channel.

A

Cloacal Extrophy

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21
Q

When is the anatomy of the GI tract developed?

A

20weeks

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22
Q

When is bile metabolism start and when does it start to be secreted?

A

11 week and 22 weeks

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23
Q

The gut is initially sterile but gut colonization is needed for…

A

vit K

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24
Q

NB have limited digestion and absorption of what three main things?

A

CHO, fats, proteins

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25
What is the main site of hematopoiesis by type II cells?
Liver
26
By the 3rd month, the liver must start to synthesis ____ and ____ so help keep the infant's Bld glucose stable.
Cholesterol and glycogen
27
What are the three sources the liver receives blood from?
hepatic portal vein, hepatic artery, and UVC through Ductus Venosus
28
What organ metabolises CHO to glucose (galactose->fructose->glucose)
Liver
29
What is bilirubin comprised of?
the end product of heme degredation and hemoglobin from dead RBCs
30
What are the three components when Hgb is brokendown?
Iron - stored in the body CO - exhaled Biliverdin - bkdn into unconjugated bilirubin
31
What type of bilirubin binds to albumin -> goes to liver (water soluble form) ->to intestines -> excreted in stool
Conjugated bilirubin
32
What is when congugated bilirubin is converted back to unconjugated bilirubin which is reabsorped back into the liver
enterohepatic re-circulation
33
What are three main causes of poor binding of bilirubin to get excreted?
low albumin drugs - compete for binding sites pH
34
What is indirect bilirubin? physiologically rises slowly in the NB
Unconjugated bilirubin
35
What is direct bilirubin? freely removed. levels increase when bile flow is obstructed.
Conjugated bilirubin
36
When a small amt of unconjugated bilirubin is not bound to albumin and could cross the BBB leading to neuronal damage?
Free bilirubin
37
Elevated levels of AST and ALT may indicate ____ ____.
hepatocyte damage
38
What is the most abundant plasma protein? the level is decreased in a damaged liver = puffy
Albumin
39
What enzymes catalyze oxidation-reduction reactions and also assess hepatic injury in the neonate?
dehydrogenase
40
What are the 4 coagulation proteins that are produced in the liver?
prothrombin, factor 7 and 10, and vit K
41
What are two key liver enzymes that metabolize drugs. expressed gradually making drug metabolism sluggish in neonates.
CYP450 and glucoronyl transferase
42
What organ produces >25 digestive proteins and is immature at birth.
Pancreas - dorsal is much larger than the ventral segment
43
When overstimulation of the islet cells from a diabetic mother leading to hypoglycemia.
Hyperinsulinemia
44
What cell type has glucogon? insulin? and somatostatin (islet cells of the pancrease)
Alpha Beta Gamma
45
When is the primary Neurulation of the fetal brain? | the Dorsal induction.
3-4weeks gest
46
Myelination usually occurs when and continues for years postnatally?
Birth
47
When is the Gyri formed? so you must wait if you are uncomfortable at 35 weeks.
38weeks
48
How do the neural folds fuse? a zipper
From cephalic to caudal direction; from the center to the head and butt
49
When does the neural tube close?
By the 4th week
50
What is seen when there is a possible open neural tube defect? Levels peak at 10-14 wks and decrease with increaaing GA
Alpha-fetoprotein
51
What NTD in the crainial area fails at 24-25days. The exposed brain tissue become necrotic from the A.F
Anencephaly
52
The failure of the Caudal part to close. a bony defect with the herniation of meninges and brain tissue thru the skull.
Encephalocele
53
When failure of the Neural tube to fold over but the back is still closed. Could have a tethered cord.
SpinaBifida Occulta
54
NTD with a sac full of meninges, spinal cord, or both. Three different types of NTD is in this group.
Spina bifida cyctica
55
S.B cyctica that has a sac with nerve roots, meninges, and CSF. Neurologic defect below the level of the sac
Meningomyelocele
56
S.B. Cyctica with a sac of just CSF and meninges. Better prognosis.
Meningocele
57
The most sever form of SB cyctica. Can be entire length of spinal cord.
Myeloschisis
58
The downward displacement of the cerebellar which can cause a blockage of CSF leading to Hydrocephalus. Cerebellat tonsils are pulled through the foramen magnum.
Arnold-Chiari malformation
59
What stage is between 5-6weeks when the brain divides into the forebrain and midbrain
Prosencephalic development
60
When does neuronal proliferation begin and it peaks at _____ wks?
begins at 8 week and peaks - 12wks
61
What are the two last areas for neuronal growth?
Cerebellum and cerebrum
62
What is when there is a decrease in the size OR number of neuronal-glial cell units? assoc. with ETOH, cocaint, PKU, and radiation
Microencephaly
63
When do the neurons reach thier permanent loaction. Differentiation is still occurring.
28 wks
64
When dose myleinization begin and peaks? Peripheral NS: Central NS:
Begins at 20wks and peaks at 6-1year old PNS - motor ->sensory CNS - Sensory -> motor
65
What can malnutrition lead to?
hyoplasia of cerebral white matter and decreased myelinization
66
What brain part has rapid growth from 24-40 weeeks. Injury to this decreases language, behavioral and cognitive function
Cerebellar development
67
VISION: myelinization of optic nerve? visual attention?
optic nerve - 25 weeks | attention - 30-32 weeks
68
How does motor tone develop? and they increase with gest age
Develops from tail to head | and from distal-proximal
69
What are four major categories an infant must have for autonomic regulation? CNS system is intact
sustaining respiration, stable HR, stable temp, and food feeding techniques
70
Where is the most common source of IVH? and usually caused by asphyixa with reperfusion and birth trauma.
Subependymal germinal matrix
71
MAP -ICP = ____ and it increases with G.A.
Cerebral perfusion pressure
72
At what age do infants respond to taste and smell? - auditory processing - pupillary responses - awake visual attention
taste - 36 auditory - 30 pupillary - 29 visual - 30
73
What refers to the brain changes in response to external experiences, ex: repeated/inappropriate stimulation
brain plasticity
74
``` Reflex: appears: 28-32 weeks disappears:6 months asymmetry = brachial plexia injury nonhabituation = cerebral injury ```
Moro
75
Reflex: appears: 28 wks disappears: 2 months nonhabituation = cerebral injury
Palmar grasp
76
Reflex: appears: 35 wks disappears: 7 months nonhabituation = cerebral abnormalities
Tonic neck
77
What is under developed and is not consistant with the demands of the environment? Sensory overload.
CNS development
78
What is when the necrotic changes in white matter that follows an ischemic episode? ongoing hypoxic episodes.
Periventricular Leukomalacia
79
When necrosis of neurons in the cortices of cerebrum and cerebellum occurs. Free radicals are formed from re-perfusion
HIE - hypoxic-ischemic encephalopathy
80
What involves massive discharge of neurons and intense energy consumption. Hypoxia, hypoglycemia, and other metabolic changes occure in the CNS
Seizures
81
When does the WBC production shift to the bone marrow?
12th week
82
When does the thymus development begin and when d the lymphocytes appear in the thymus?
4th week and then the 8th week
83
What is the main mission of the immune system?
Detect, destroy, and eliminate foreign materals.
84
What is the response of the immune system when the body is exposed to a foreign antigen?
Active immunity
85
What is the acquired immunity that results from active immunity? Memory cells are established.
Adaptive immunity
86
What are the cell-mediated factors that includes helper cells, cytotoxic cells, and suppressor cells?
T lymphocytes
87
What are the humoral factors that includes all the immunoglobulins (IgG, IgD, IgM, IgE, IgA)
B Lymphocytes
88
Which immunity has memory? The body remembers the particular invader so the response is higher the 2nd go round.
Adaptive immunity
89
What are proteins that react with specific antigens. They bind to invading pathogens to be reecognized as a foreign
Antibodies