• Wrong document? Swap it for free
  • Written by students who passed
  • Immediately available after payment
  • Read online or as PDF
Sell
Where do you study
Your language
Document preview thumbnail
Preview 2 out of 7 pages
Exam (elaborations)

Nsg 530/Nsg 530 Exam 1 Latest 2024 With Actual Questions And Correct Verified Answers/Already Graded A+ 100% Guaranteed To Pass Concepts(All What You Need) Latest Edition 2024

Document preview thumbnail
Preview 2 out of 7 pages

NSG 530/NSG 530 EXAM 1 LATEST 2024 WITH ACTUAL QUESTIONS AND CORRECT VERIFIED ANSWERS/ALREADY GRADED A+ 100% GUARANTEED TO PASS CONCEPTS(ALL WHAT YOU NEED) LATEST EDITION 2024

Content preview

NSG 530/NSG 530 EXAM 1 LATEST 2024 WITH ACTUAL QUESTIONS
AND CORRECT VERIFIED ANSWERS/ALREADY GRADED A+ 100%
GUARANTEED TO PASS CONCEPTS(ALL WHAT YOU NEED) LATEST
EDITION 2024




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


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
Affects both sexes
Intellectual disability, poor muscle tone, low nasal bridge, low set ears,
protruding tongue, epicanthal fold

Document information

Uploaded on
September 16, 2024
Number of pages
7
Written in
2024/2025
Type
Exam (elaborations)
Contains
Questions & answers
$26.49

Wrong document? Swap it for free Within 14 days of purchase and before downloading, you can choose a different document. You can simply spend the amount again.
Written by students who passed
Immediately available after payment
Read online or as PDF

Seller avatar
Reputation scores are based on the amount of documents a seller has sold for a fee and the reviews they have received for those documents. There are three levels: Bronze, Silver and Gold. The better the reputation, the more your can rely on the quality of the sellers work.
trustednurse
4.9
(2504)
Sold
972
Followers
413
Items
11503
Last sold
1 day ago




Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their tests and reviewed by others who've used these notes.

Didn't get what you expected? Choose another document

No worries! You can instantly pick a different document that better fits what you're looking for.

Pay as you like, start learning right away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and aced it. It really can be that simple.”

Alisha Student

Working on your references?

Create accurate citations in APA, MLA and Harvard with our free citation generator.

Working on your references?

Frequently asked questions