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Pathophysiology D115 WGU Study Guide Exam 2024/2025 with Questions and Verified Rationalized Answers Guaranteed Pass $15.49
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Pathophysiology D115 WGU Study Guide Exam 2024/2025 with Questions and Verified Rationalized Answers Guaranteed Pass

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Pathophysiology study guide WGU D115 exam preparation Pathophysiology exam questions 2024 pathophysiology exam guide Verified exam answers pathophysiology WGU pathophysiology test help D115 pathophysiology exam tips Pathophysiology rationalized answers Study guide D115 WGU 2025 Pathophysio...

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  • December 22, 2024
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  • 2024/2025
  • Exam (elaborations)
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  • wgu d115 exam preparation
  • wgu pathophys
  • D115 WGU
  • D115 WGU
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Pathophysiology D115 WGU Study Guide Exam 2024/2025
with Questions and Verified Rationalized Answers Guaranteed Pass




1. Turner Syndrome: A chromosomal disorder in females in which either an X chromos
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ome is missing, making the person XO instead of XX, or part of one X chromosome is del
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eted.
2. Tay-
Sachs disease: A human genetic disease caused by a recessive allele that leads to the accu
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mulation of certain lipids in the brain. Seizures, blindness, and degeneration of motor and m
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ental performance usually become manifest a few months after birth.
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3. Down Syndrome: a condition of mild to severe intellectual disability and associ-
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v ated physical disorders caused by an extra copy of chromosome 21
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4. Marfan Syndrome: autosomal dominant trait.. v v v v




a genetic disorder that changes the proteins that help make healthy connective tissue. T
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his leads to problems with the development of connective tissue, which supports the bo
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nes, muscles, organs, and tissues in your body.
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5. Marfans syndrome genetic trait type: Autosomal dominant. inherited in an autosomal p
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attern which means one copy of the altered gene in each cell is sufficient to cause the disorder.
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6. What causes Marfan's syndrome?: Defects or deletions (pathogenic variants) of the fib
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rillin-1 (FBN1) gene have been shown to cause Marfans syndrome
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at least 25% of Marfan syndrome cases result from a new mutation in the FBN1 gene
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7. spina bifida: a congenital defect that occurs during early pregnancy when the spinal ca
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1v/v20

,nal fails to close completely around the spinal cord to protect it
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8. What can cause Spina Bifida: Decreased folic acid or maternal use of valproic acid
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9. Turner syndrome characteristics: Underdeveloped ovaries (sterile) Short st
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ature (~ 4'7")
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Webbing of the neck Edema v v v v



Underdeveloped breasts; wide nipples High nu v v v v v



mber of aborted fetuses
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10. Diagnostic testing for Turner's syndrome: genetic testing , echo, bone densi-
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v ty, and bone age testing are necessary.
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11. Treatment of Turners syndrome: Treatment involves estrogen therapy and growth hor
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mone administration. Treat symptomatically for all other effects of the dz.
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12. Cushing's Syndrome: a condition caused by prolonged exposure to high levels of cortisol
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2v/v20

, 13. Cushing syndrome symptoms: fatty hump between shoulders, a rounded face(moon f
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aced), and pink or purple stretch marks on skin, thinning fragile skin, slow healing of cuts, ins
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ect bites and infections, acne, decreased libido, decreased fertility, irregular or absent mens
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trual periods, fatigue, muscle weakness, cognitive difficulties, and headaches.
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14. Viral hemorragic fevers: spread by contact with infected animals or insects. Most co
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mmon hosts are mosquitos, ticks, rodents, or bats.
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15. MRSA (methicillin- v



resistant Staphylococcus aureus): an infection caused by specific bacteria that has becom
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e resistant to many antibiotics
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16. B12 anemia: cobalamin deficiency, is a condition that develops when your body can't ma
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ke enough healthy red blood cells because it doesn't have enough vitamin B12. Your body ne
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eds vitamin B12 to make healthy red blood cells, white blood cells, and platelets. (pernicious a
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nemia)
17. Pernicious Anemia: a type of vitamin B12 anemia. An autoimmune condition in which t
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he body's immune system attacks the actual intrinsic factor (IF) protein or the cells in the lini
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ng of your stomach that make it.
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18. Folate (folic acid) deficiency anemia: - v v v v v



v Folate is an essential vitamin for RNA and DNA synthesis within maturing RBC
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- Absorption of folate occurs in the upper small intestine v v v v v v v v




- Is common in alcoholics and individuals with chronic malnourishment
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- Is associated with neural tube defects of the fetus
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Folate deficiency occurs when your body doesn't get enough folate. Symptoms include fatigu
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3v/v20

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