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Curricular information is subject to change
On completion of this module you will be able to:- Understand what is meant by the term rare disease - Consider the issues associated with managing patients and their families with rare genetic disorders - For selected rare genetic disorders, demonstrate scientific knowledge of the inheritance patterns and implications for family members and their children. - Appreciate the importance of research to diagnosis of rare diseases and the importance of identifying novel treatments for these orphan genetic disorders - Rationalise the current Governmental Health Policies and funding initiatives to support Rare Disease Research. - Identify the resources currently available for Health Care professionals to access information on rare diseases and identify the health educational gaps in this regard
Student Effort Type | Hours |
---|---|
Lectures | 24 |
Specified Learning Activities | 30 |
Autonomous Student Learning | 60 |
Total | 114 |
Students are required to have a background in human genetics
Learning Recommendations:This module is an ideal complement to the core stage 3 module, Genetics, Perinatal and Paediatric Diseases
Resit In | Terminal Exam |
---|---|
Autumn | No |
• Group/class feedback, post-assessment
Not yet recorded.
Lecture | Offering 1 | Week(s) - 20, 21, 22, 23, 24, 25, 26, 29, 30, 31, 32, 33 | Thurs 16:00 - 17:50 |
Lecture | Offering 1 | Week(s) - 20, 21, 29, 30, 31, 32, 33 | Tues 15:00 - 15:50 |
Lecture | Offering 1 | Week(s) - 22 | Tues 15:00 - 15:50 |
Lecture | Offering 1 | Week(s) - 23, 24, 25, 26 | Tues 15:00 - 15:50 |