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NSG530 / NSG 530 Exam 1 | Advanced Pathophysiology | Questions & Verified Answers with Rationales | 100% Correct | Grade A+

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NSG530 / NSG 530 Exam 1 | Advanced Pathophysiology | Questions & Verified Answers with Rationales | 100% Correct | Grade A+

Institution
NSG530 / NSG 530
Course
NSG530 / NSG 530

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1



NSG530 / NSG 530 Exam 1 | Advanced
Pathophysiology | Questions & Verified Answers with
Rationales | 100% Correct | Grade A+
Interphase - (ANSWER)cell feeds, metabolizes and grows while replicating DNA in
preparation for mitosis



Prophase - (ANSWER)first appearance of chromosomes (will be 92)



Metaphase - (ANSWER)Centrioles pull chromosomes to opposite sides of cell
(chromatid) - 46 each side



Anaphase - (ANSWER)Centromeres split and sister chromatids are pulled apart



Telophase - (ANSWER)New nuclear membrane formed around each group of 46
chromosomes *When it goes right, euploid cells are produced*



Nondisjunction - (ANSWER)Error in meiosis in which homologous chromosomes
fail to separate.



Polyploidy - (ANSWER)condition in which an organism has extra sets of
chromosomes



Triploidy - (ANSWER)when an organism has three copies of every chromsome
instead of two

, 2




Tetrapoloidy - (ANSWER)euploid has 92 chromosomes and fetus usually does not
survive



Huntington's disease - (ANSWER)Single gene disorder (trinucleotide repeat
mutation)

Autosomal dominant (50% chance of passing it on)

Progressive neurologic disease with late onset (40s)

Prevention- genetic testing for pregnancy planning



Cystic fibrosis - (ANSWER)Single gene disorder (CFTR gene mutation)

Autosomal recessive

Most common in white children

Defective transport of chloride ions cause salt imbalance- thickened secretions,
digestive issues, malnutrition. Males and females

Must inherit two copies of gene (1 from each parent)



Turner syndrome - (ANSWER)XO chromosomal disorder, monosomy of X-affects
females

Short stature, webbed neck, undeveloped breasts but female genitalia, usually
sterile



Down syndrome - (ANSWER)Chromosomal disorder, trisomy 21

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