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NR 283 Pathophysiology Exam 1 – Qualified Questions and Answers Study Guide

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This study guide covers the foundational concepts typically tested in NR 283 Pathophysiology Exam 1, including cellular function, cellular injury, inflammation, immunity, genetics, fluid and electrolyte balance, acid-base regulation, and stress responses. It contains qualified practice questions with detailed answers designed to strengthen understanding of disease processes and prepare students for nursing examinations. The material is organized for efficient review and supports both conceptual learning and clinical application.

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NR 283 PATHOPHYSIOLOGY
Course
NR 283 PATHOPHYSIOLOGY

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NR 283 PATHOPHYSIOLOGY EXAM 1
WITH QUALIFIED QUESTIONS AND
ANSWERS
Etiology - ANSWER-Cause of particular disease on microscopic level



Pathogenesis - ANSWER-Story of how disease develops



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

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NR 283 PATHOPHYSIOLOGY
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