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Examen

AGILE SAFE EXAM PREP 2026 TEST PAPER QUESTIONS AND ACCURATE ANSWERS

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AGILE SAFE EXAM PREP 2026 TEST PAPER QUESTIONS AND ACCURATE ANSWERS

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AGILE SAFE EXAM PREP 2026 TEST PAPER
QUESTIONS AND ACCURATE ANSWERS

▶ Passive natural immunity . Answer: mother to fetus

▶ Passive artificial immunity . Answer: adult antibody injected into another
adult


▶ Atrophy . Answer: Decrease in the size of the cells, results in reduced
tissue mass

▶ Hypertrophy . Answer: Increase in cell size, results in enlarged tissue
mass

▶ Hyperplasia . Answer: Increased number of cells, results in enlarged
tissue mass

▶ Metaplasia . Answer: Mature cell type is replaced by a different mature
cell type, Ex: chronic smokers, cells lose cilia

▶ Dysplasia . Answer: Cells are different looking varying in size and shape

▶ Neoplasia . Answer: New growth, commonly a tumor. May be malignant
or benign

▶ Apoptosis . Answer: Programmed cell death, normal occurrence in the
body

▶ Ischemia . Answer: Deficit of oxygen in the cells

▶ Hypoxia . Answer: Reduced oxygen in the tissues

▶ Iatrogenic . Answer: illness or disease process because a medical
process was done ex: CAUTI

,▶ Autosomal Recessive Disorders . Answer: Has to have two recessive
genes to have disease, only one recessive gene to be carrier ex: Cystic
fibrosis, PKU (phenylketonuria), Tay-Sachs

▶ Cystic fibrosis . Answer: autosomal recessive disorder that causes thick
mucous secretions

▶ PKU (phenylketonuria) . Answer: autosomal recessive disorder that
causes an inability to metabolize phenylalanine. Can cause mental
retardation. Pt must follow strict very low protein diet

▶ Tay-Sachs . Answer: autosomal recessive disorder that causes an
enzyme to not be produced causing fatty proteins build up causing
destruction of nerve cells in the brain and spinal cord

▶ Autosomal Dominant Disorders . Answer: Only takes one gene for
disease to show. There are no carriers, either have disease or don't.
Marfan Syndrome, Huntington's, Familial Hypercholesterolemia

▶ Marfan Syndrome . Answer: Autosomal Dominant Disorder, causes long
extremities, congenital heart defects

▶ Huntington's Disease . Answer: Autosomal Dominant Disorder, nerve
cells break down over time, causing involuntary movements

▶ Familial Hypercholesterolemia . Answer: Autosomal Dominant Disorder,
high cholesterol

▶ X-Linked Disorders . Answer: Disorder carried on the x chromosome

▶ Recessive X-Linked Disorders . Answer: Color blindness, more
prominent in males, XcY male color blind, XcXc female color blind. XcX not
color blind only carrier.

▶ Chromosomal Disorder . Answer: not inherited, theres a problem on the
chromosome

▶ Types of Chromosomal Disorders . Answer: Down's Syndrome, Turner
Syndrome, Klinefelter Syndrome

, ▶ Down's Syndrome . Answer: Trisomy 21

▶ Turner Syndrome . Answer: Only affects females, short stature, infertility,
XO

▶ Klinefelter Syndrome . Answer: Only affects males, develop breasts and
small testes, extra X chromosome present XXY

▶ Intracellular Fluid . Answer: Fluid inside the cell, accounts for 2/3 of body
water

▶ Extracellular Fluid . Answer: Fluid outside the cell, IVF (intravascular fluid
or blood plasma), ISF (interstitial fluid or fluid between tissues and blood),
CSF, and Transcellular fluid (Synovial, Pericardial cavities)

▶ Hydrostatic Pressure . Answer: Push, typically happens at the arterial
level

▶ Osmotic Pressure . Answer: Pull, typically on the veinous level, wherever
the waste needs to be eliminated from the body

▶ Isotonic Solutions . Answer: Completely balanced solutions, blood, NS

▶ Hypotonic Solutions . Answer: Less solute so its less concentrated, only
a few pepper flakes, 0.45% NaCl (1/2 NS)
Give this to dehydrated pt

▶ Hypertonic Solutions . Answer: More solute, so its more concentrated,
lots of pepper flakes, 3.0-5.0% NaCl
Give this to cerebral edema pt

▶ Na+ Normal Range . Answer: 135-145 mEq/L

▶ K+ Normal Range . Answer: 3.5-5.0 mEq/L

▶ Cl- Normal Range . Answer: 98-106 mEq/L

▶ Ca2+ Normal Range . Answer: 8.5-10.5 mEq/L

Información del documento

Subido en
11 de marzo de 2026
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Escrito en
2025/2026
Tipo
Examen
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