|Year of offer||2019|
|Subject level||Graduate coursework|
|Fees||Subject EFTSL, Level, Discipline & Census Date|
This subject will examine the roles of both genetic and environmental determinants in the expression of complex disease traits and cancer. Principles of genetic and genomic testing will be investigated and students will learn to apply these in clinical case-based scenarios.
This curriculum is based on the genetic knowledge requirements of the Human Genetics Society of Australasia (HGSA Board of Censors for Genetic Counselling, which governs the certification of genetic counsellors in Australia. The course will be delivered via a combination of on-line content and case-based face-to-face tutorials.
Intended learning outcomes
- Discuss the causes of neural tube & other birth defects;
- Explain the role of genetic & environmental determinants in complex human diseases;
- Analyse patient & family history to assess inherited cancer predisposition;
- Explain testing options available for suspected genetic conditions;
- Interpret and apply genetic and genomic reports to develop sound clinical recommendations.
On completing this subject students should be able to:
- Understand the role of genetics as the underlying cause of various disorders of the human body
- Understand the role of genetics in cancer
- Have an appreciation for the role of the genetic counsellor in the context of the multidisciplinary approach to clinical genetic health care
- Understand the principles of the legal and professional duties and responsibilities of genetic counsellors as health professionals and members of a health care team
- Have an appreciation for the approaches to treatment for specific genetic disorders