DNP 810 WEEK 3 CASE REPORT PART 2 GCU

1. DNP 810 WEEK 3 CASE REPORT PART 2 GCU Just Click on Below Link To Download This Course: https://www.tutorialsexperts.com/product/dnp-810-week-3-case-report-part- 2-gcu/ Or Email us HELP@TUTORIALSEXPERTS.COM Details: You will be creating a case report in stages over four course topics. This assignment will add to your previous work in Topic 2. Use an example from your own personal practice, experience, or own personal/family; however, simulated cases are not acceptable for practice hours and therefore not acceptable for this assignment. Examples might include a patient with Duchesne’s muscular dystrophy. Huntington’s disease, Down’s syndrome, sickle cell anemia, BRCA 1 or BRCA 2 mutations, or other genetic disorder that you and/or the organization you practice in may specialize in treating. General Requirements: Use the following information to ensure successful completion of the assignment:  This assignment uses a rubric. Please review the rubric prior to beginning the assignment to become familiar with the expectations for successful completion. Doctoral learners are required to use APA style for their writing assignments. The APA Style Guide is located in the Student Success Center. This assignment requires that at least two additional scholarly research sources related to this topic, and at least one in-text citation from each source be included. You are required to submit this assignment to LopesWrite. Please refer to the directions in the Student Success Center.    Directions: For this assignment (Part 2 of the Case Report), write a 1,000-1,250 word paper incorporating genetics information learned from assigned readings in Topics 1-3. Include the following: 1. Describe if chromosomal analysis is/was indicated. 2. Detail the causes of the disorder. 3. Describe the disorder in terms of its origin as either a single gene inheritance, or as a complex inheritance and considerations for practice and patient education.

2. 4. Analyze the gene mutation of the disease, as well as whether it is acquired or inherited, and how the mutation occurs. Portfolio Practice Hours: Practice immersion assignments are based on your current course objectives, and are intended to be application-based learning using your real-world practice setting. These assignments earn practice immersion hours, and are indicated in the assignment by a Portfolio Practice Hours statement which reminds you, the student, to enter in a corresponding case log in Typhon. Actual clock hours are entered, but the average hours associated with each practice immersion assignment is 10. You are required to complete your assignment using real-world application. Real-world application requires the use of evidence-based data, contemporary theories, and concepts presented in the course. The culmination of your assignment must present a viable application in a current practice setting. For more information on parameters for practice immersion hours, please refer to DNP resources in the DC Network. To earn portfolio practice hours, enter the following after the references section of your paper: Practice Hours Completion Statement DNP-810 I, (INSERT NAME), verify that I have completed (NUMBER OF) clock hours in association with the goals and objectives for this assignment. I have also tracked said practice hours in the Typhon Student Tracking System for verification purposes and will be sure that all approvals are in place from my faculty and practice mentor. Case Report: Part 2 2 Less Than Satisfactory 74.00% 1 Unsatisfactory 0.00% 3 Satisfactory 79.00% 4 Good 87.00% 5 Excellent 100.00% 70.0 %Content Discussion of whether or not chromosomal analysis is/was indicated is clearly present and convincing. Information presented is from scholarly though dated sources. Discussion of the causes of the disorder is clearly present and convincing. Information presented is Discussion of whether or not chromosomal analysis is/was indicated is clearly present and insightful. Information presented is from current scholarly sources. Discussion of whether or not chromosomal analysis is/was indicated is not present. 10.0 %Description of Whether or Not Chromosomal Analysis Is/Was Indicated Discussion of whether or not chromosomal analysis is/was indicated is present but incomplete. Discussion of whether or not chromosomal analysis is/was indicated is present but done at a perfunctory level. Discussion of the causes of the disorder is not present. Discussion of the causes of the disorder is present but incomplete. Discussion of the causes of the disorder is present but done at a perfunctory level. Discussion of the causes of the disorder is clearly present and insightful. Information presented is 20.0 %Discussion of the Causes of the Disorder

3. from scholarly though dated sources. Description of the disorder in terms of its origin as either a single gene inheritance, or as a complex inheritance and considerations for practice and patient education is clearly presented and convincing. Information presented is from mostly current scholarly but some outdated sources are used. Analysis of the gene mutation of the disease, as well as whether it is acquired or inherited, and how the mutation occurs is clearly presented. Discussion is convincing. Information presented is from mostly current scholarly but some outdated sources are used. from current scholarly sources. Description of the disorder in terms of its origin as either a single gene inheritance, or as a complex inheritance and considerations for practice and patient education is clearly presented, insightful and detailed. Information presented is from current scholarly sources. Description of the disorder in terms of its origin as either a single gene inheritance, or as a complex inheritance and considerations for practice and patient education is presented but incomplete. 20.0 %Description of the Disorder in Terms of Its Origin as Either a Single Gene Inheritance, or as a Complex Inheritance and Considerations for Practice and Patient Education Description of the disorder in terms of its origin as either a single gene inheritance, or as a complex inheritance and considerations for practice and patient education is not presented. Description of the disorder in terms of its origin as either a single gene inheritance, or as a complex inheritance and considerations for practice and patient education is presented but done at a perfunctory level. Analysis of the gene mutation of the disease, as well as whether it is acquired or inherited, and how the mutation occurs is clearly presented. Discussion is insightful and detailed. Information presented is from current scholarly sources. Analysis of the gene mutation of the disease, as well as whether it is acquired or inherited, and how the mutation occurs is presented. Discussion is incomplete. Analysis of the gene mutation of the disease, as well as whether it is acquired or inherited, and how the mutation occurs is presented. Discussion is done at a perfunctory level. 20.0 %Analysis of the Gene Mutation of the Disease, as Well as Whether It Is Acquired or Inherited, and How the Mutation Occurs Analysis of the gene mutation of the disease, as well as whether it is acquired or inherited, and how the mutation occurs is not presented. 20.0 %Organization and Effectiveness Thesis and/or main claim are clear and forecast the development of the paper. It is descriptive and reflective of the arguments and appropriate to the purpose. Thesis and/or main claim are comprehensive. The essence of the paper is contained within the thesis. Thesis statement makes the purpose of the paper clear. Thesis and/or main claim are insufficiently developed and/or vague; purpose is not clear. Paper lacks any discernible overall purpose or organizing claim. 7.0 %Thesis Development and Purpose Thesis and/or main claim are apparent and appropriate to purpose. Argument is orderly, but may have a few inconsistencies. The argument presents minimal justification of claims. Argument logically, but not thoroughly, supports the purpose. Sources used are credible. Introduction and conclusion bracket the thesis. Some mechanical errors or typos are present, but are not overly distracting to the reader. Correct sentence structure and Sufficient justification of claims is lacking. Argument lacks consistent unity. There are obvious flaws in the logic. Some sources have questionable credibility. Argument shows logical progressions. Techniques of argumentation are evident. There is a smooth progression of claims from introduction to conclusion. Most sources are authoritative. Statement of purpose is not justified by the conclusion. The conclusion does not support the claim made. Argument is incoherent and uses noncredible sources. Clear and convincing argument that presents a persuasive claim in a distinctive and compelling manner. All sources are authoritative. 8.0 %Argument Logic and Construction Surface errors are pervasive enough that they impede communication of meaning. Frequent and repetitive mechanical errors distract the reader. Inconsistencies in Prose is largely free of mechanical errors, although a few may be present. A variety of sentence structures and 5.0 %Mechanics of Writing (includes spelling, punctuation, Writer is clearly in command of standard, written, academic English.

4. grammar, language use) Inappropriate word choice and/or sentence construction are used. language choice (register), sentence structure, and/or word choice are present. audience-appropriate language are used. effective figures of speech are used. 10.0 %Format Appropriate template is used, but some elements are missing or mistaken. A lack of control with formatting is apparent. Template is not used appropriately or documentation format is rarely followed correctly. Appropriate template is used. Formatting is correct, although some minor errors may be present. 5.0 %Paper Format (Use of appropriate style for the major and assignment) Appropriate template is fully used. There are virtually no errors in formatting style. All format elements are correct. 5.0 %Research Citations (In-text citations for paraphrasing and direct quotes, and reference page listing and formatting, as appropriate to assignment and style) 100 %Total Weightage Reference page is included and lists sources used in the paper. Sources are appropriately documented, although some errors may be present. Reference page is present and fully inclusive of all cited sources. Documentation is appropriate and citation style is usually correct. In-text citations and a reference page are complete and correct. The documentation of cited sources is free of error. No reference page is included. No citations are used. Reference page is present. Citations are inconsistently used. Download File