| Code |
13527
|
| Year |
1
|
| Semester |
S2
|
| ECTS Credits |
6
|
| Workload |
TP(60H)
|
| Scientific area |
Biomedical Sciences
|
|
Entry requirements |
None
|
|
Mode of delivery |
Face to face (theoretical, theoretical-practical and laboratorial)
|
|
Work placements |
Not applicable
|
|
Learning outcomes |
This Curricular Unit (CU) aims to provide students with general knowledge of comprehensive and updated principles of genetics and fundamental molecular mechanisms that lead to human genetic diseases.
This CU was planned in order to provide students with knowledge and skills in Human Genetics. So, at the end of this CU, students must:
- Know the evolution of Human Genetics over time;
- Remember the Mendelian Genetics and Cytogenetics fundamentals;
- Know the techniques of genetic and physical mapping of the human genome;
- Identify the genetic variants that influence human health;
- Understand the Molecular Genetics underlying muscle, neurological, ocular and mitochondrial disorders, among others;
- be able to perform molecular genetics techniques at the laboratory level, particularly regarding the genetic diagnosis of MODY diabetes (Maturity-Onset Diabetes of the Young);
- Understand the importance of Clinical Genetics and genetic diagnosis.
|
|
Syllabus |
- Human Molecular Genetics foundations
- Genetic and physical mapping of human chromosomes
- Epigenetics
- Organism models in the study of genetic diseases
- Analysis of human monogenic diseases
- Complex Genetic Diseases: identification of susceptibility factors and understanding of pathogenesis
- Analysis of the Molecular Genetics of selected genetic diseases:
Molecular Genetics of muscle disorders
Molecular Genetics of neurological disorders
Molecular Genetics of eye disorders
Molecular Genetics of mitochondrial disorders
- Molecular diagnoses and Clinical Genetics
|
|
Main Bibliography |
New Clinical Genetics fourth edition (4th ed.). edited by Read, A., & Donnai, D. Scion Publishing, 2020.
The Online Metabolic and Molecular Bases of Inherited Disease editado por David Valle, Arthur L. Beaudet, Bert Vogelstein, Kenneth W. Kinzler, Stylianos E. Antonarakis, Andrea Ballabio, K. Michael Gibson, Grant Mitchell. McGraw-Hill Companies, Inc. 2020
Strachan, T., & Read, A. (2018). Human Molecular Genetics: 5th Edition. CRC Press.
Speicher, M. R., Antonarakis, S. E., Motulsky, A. G., and Vogel, F. (eds) (2010). Vogel and Motulsky’s Human Genetics: Problems and Approaches. 4th completely rev. ed. Heidelberg; New York: Springer.
Pasternak, J.J. (2005) Introduction to human molecular genetics - mechanisms of inherited diseases, 2nd edition. John Wiley and Sons, Ltd.
OMIM; pubMed.
|
|
Teaching Methodologies and Assessment Criteria |
This curricular unit (CU) starts with some lectures that will provide the theoretical basis on the Molecular Genetics underlying Human Inherited Diseases (muscle, neurological, ocular and mitochondrial disorders). This theoretical knowledge will be assessed in a written test, at the end of the semester (50% of final grade).
Students will also write a review work on "Human Inherited Diseases and Nutrition" (25% of final grade) that will be presented by oral communication (25% of final grade). At this stage, students must be able to use all the knowledge and skills acquired in the course of this CU.
|
|
Language |
Portuguese. Tutorial support is available in English.
|