Pathophysiology Exam 1 South College REVISED AND
UPDATED FOR 2026/2027 ACTUAL EXAM COMPLETE
QUESTIONS AND CORRECT DETAILED ANSWERS (VERIFIED
ANSWERS) |ALREADY GRADED A+||BRAND NEW!!
Practice questions for this set
Terms in this set (50)
Which organelle, after protein synthesis is Golgi
apparatus completed, is responsible for proteins to get
packaged, processed and secreted?
A patient has an abnormal thickening of the Treatment with hormone
therapy lining of the uterus due to an increase in
estrogen levels. How can such a condition
be reversed?
, A client is diagnosed with a condition in Hypoxia
which the brain cells cannot withstand low
oxygen delivery long enough for cell
reversible changes to happen. Identify the
condition.
What does a pulse oximeter measure? Saturation of hemoglobin with oxygen (SaO2)
By which process are findings identified that Pathognomonic
changes represent distinct disease processes to help
with diagnosis?
During an endoscopic examination on a Barrett's esophagus
patient, it is found that the client has acid
reflux. Which condition associated
with gastroesophageal reflux disease
(GERD) warrants close monitoring and
aggressive treatment?
A patient is diagnosed with failure of the Hashimoto thyroiditis
thyroid gland due to increase in apoptotic
cell death causing hypothyroidism. Which
terminology do you expect to be applied
to the patient's condition?
Which aspects of polymerase chain All of the answers are correct about
PCR reaction or PCR are CORRECT?
Familial hypercholesterolemia is a genetic Children are at risk for early acute myocardial infraction
autosomal dominant disorder characterized
by a high cholesterol level. Which
statement is TRUE regarding this
condition?
Which of the genetic diseases below is an X- G6PD
deficiency linked trait that primarily affects men and
can cause acute hemolytic anemia?
Which of the following diseases is Huntington disease
autosomal dominant and will cause
movement and cognitive disorders that
begin in adulthood?
A 40 year old patient presents with mild Huntington's disease
chorea that seems to be progressing.
Genetic testing revealed a defect of the HTT
gene. What is the patient's diagnosis?
UPDATED FOR 2026/2027 ACTUAL EXAM COMPLETE
QUESTIONS AND CORRECT DETAILED ANSWERS (VERIFIED
ANSWERS) |ALREADY GRADED A+||BRAND NEW!!
Practice questions for this set
Terms in this set (50)
Which organelle, after protein synthesis is Golgi
apparatus completed, is responsible for proteins to get
packaged, processed and secreted?
A patient has an abnormal thickening of the Treatment with hormone
therapy lining of the uterus due to an increase in
estrogen levels. How can such a condition
be reversed?
, A client is diagnosed with a condition in Hypoxia
which the brain cells cannot withstand low
oxygen delivery long enough for cell
reversible changes to happen. Identify the
condition.
What does a pulse oximeter measure? Saturation of hemoglobin with oxygen (SaO2)
By which process are findings identified that Pathognomonic
changes represent distinct disease processes to help
with diagnosis?
During an endoscopic examination on a Barrett's esophagus
patient, it is found that the client has acid
reflux. Which condition associated
with gastroesophageal reflux disease
(GERD) warrants close monitoring and
aggressive treatment?
A patient is diagnosed with failure of the Hashimoto thyroiditis
thyroid gland due to increase in apoptotic
cell death causing hypothyroidism. Which
terminology do you expect to be applied
to the patient's condition?
Which aspects of polymerase chain All of the answers are correct about
PCR reaction or PCR are CORRECT?
Familial hypercholesterolemia is a genetic Children are at risk for early acute myocardial infraction
autosomal dominant disorder characterized
by a high cholesterol level. Which
statement is TRUE regarding this
condition?
Which of the genetic diseases below is an X- G6PD
deficiency linked trait that primarily affects men and
can cause acute hemolytic anemia?
Which of the following diseases is Huntington disease
autosomal dominant and will cause
movement and cognitive disorders that
begin in adulthood?
A 40 year old patient presents with mild Huntington's disease
chorea that seems to be progressing.
Genetic testing revealed a defect of the HTT
gene. What is the patient's diagnosis?
