Learning Outcomes:
On successful completion of this module, students will be able to:
1. Explain the involvement of genetics in cellular and individual diversity.
2. Understand basic chromosome biology, and the common clinical chromosome disorders
3. Understand typical and atypical mechanisms of disease inheritance, with examples
4. Understand basic molecular genetics, and the principles of diagnostic genetic testing
5. Appreciate the impact of genetic disease on families
6. Understand the principles of polygenic inheritance, with examples
7. Appreciate the causes of congenital malformations
8. Appreciate the impact of the human genome project on medicine
9. Have an insight into the current genetic techniques and technologies and future developments
Indicative Module Content:
Draft list of Module Lectures
Introduction to Medical Genetics
Basic cytogenetics
Clinical cytogenetic disease
Basic Molecular Genetics
Autosomal Dominant inheritance
Autosomal recessive inheritance
X linked disorders
Triplet repeat disorders
Haemoglobinopathies
Diagnostic Molecular Genetics
Cancer genetics
Congenital anomalies
Biochemical Genetics
Molecular cytogenetics
Genetic imprinting
Polygenic disease
Clinical Genetics
Cystic Fibrosis (CF) - the patient experience
Population Genetics and risk calculation
Genetic counselling
Clinical Symposium Haemochromatosis
Genetic counselling - demonstration
Gene therapy
Ethical Issues in genetics
Genetics in the future