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Posted: July 7th, 2022
Genetic Mutation Assignment Instructions
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.
Please use the following headings/subheadings as a guide to
draft your paper:
Introduction (including a brief purpose statement)
Identify the genetic mutation responsible for fragile X-associated
mental retardation.
Describe and discuss how it causes the clinical syndrome of
developmental delay, joint hyperextensibility, large testes, and
facial abnormalities.
Identify which parent is the probable carrier of the genetic
mutation?
Explain why this parent and the grandparents are phenotypically
unaffected.
Discuss the likelihood that the unborn child will be affected?
Conclusion
In regards to APA format, please use the following as a guide:
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