Identify which parent is probable carrier of the mutation


Homework

Lisa Anderson, a 22 y.o., Caucasian single parent, is referred for genetic counseling by her pediatric Nurse Practitioner. She has a 3-year-old boy with developmental delay and small joint hyperextensibility. The pediatric Nurse Practitioner has diagnosed fragile X-associated mental retardation. She is currently pregnant with her second child at 14 weeks of gestation. The family history is unremarkable.

Use the following headings/subheadings as a guide to draft your paper:

A. Introduction (including a brief purpose statement)

B. Identify the genetic mutation responsible for fragile X-associated mental retardation.

C. Describe and discuss how it causes the clinical syndrome of developmental delay, joint hyperextensibility, large testes, and facial abnormalities.

D. Identify which parent is the probable carrier of the genetic mutation?

E. Explain why this parent and the grandparents are phenotypically unaffected.

F. Discuss the likelihood that the unborn child will be affected?

G. Conclusion.

Format your homework according to the give formatting requirements:

1. The answer must be double spaced, typed, using Times New Roman font (size 12), with one-inch margins on all sides.

2. The response also includes a cover page containing the title of the homework, the course title, the student's name, and the date. The cover page is not included in the required page length.

3. Also include a reference page. The references and Citations should follow APA format. The reference page is not included in the required page length.

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