Course Details

DISEASE & GENETICS

MBG435

Course Information
SemesterCourse Unit CodeCourse Unit TitleT+P+LCreditNumber of ECTS Credits
5MBG435DISEASE & GENETICS3+0+035

Course Details
Language of Instruction English
Level of Course Unit Bachelor's Degree
Department / Program BIOENGINEERING
Type of Program Formal Education
Type of Course Unit Elective
Course Delivery Method Face To Face
Objectives of the Course The aim of this course is to provide basic knowledge and skills to understand the molecular and cellular basis of inherited genetic disorders. It is aimed for students to develop a comprehensive understanding of the causes, clinical manifestations, diagnostic methods and current or developing treatment strategies of genetic diseases. In addition, it is aimed for students to evaluate ethical, social and psychological dimensions by analyzing the effects of genetic disorders on individuals and society.
Course Content This course provides an in-depth review of human genetic disorders, covering their causes, symptoms, diagnosis, and treatment options. Students will gain a comprehensive understanding of the basic genetic mechanisms that contribute to various disorders and their impact on individuals and society.
Course Methods and Techniques Basic concepts and theoretical information are directly transferred by the instructor.

It is used especially in the introductory topics of the course (atomic structure, macromolecules, cell components, etc.).

Advantage: A lot of information is transferred in a short time.
Questions and answers are used to increase the active participation of students in the course.

It is applied at the end of the subject or during the course to gather the attention of the students and reinforce the information.
Prerequisites and co-requisities None
Course Coordinator None
Name of Lecturers Instructor Dr. Demet Şaylan
Assistants None
Work Placement(s) No

Recommended or Required Reading
Resources Thompson & Thompson Genetics in Medicine
This course comprehensively examines the molecular basis, classification, diagnostic methods and treatment approaches of human genetic disorders. Students learn about genetic structures extending from DNA to genes and chromosomes, mutations and epigenetic mechanisms that play a role in the formation of hereditary diseases. They also recognize various types of genetic diseases such as monogenic and chromosomal disorders; and analyze the biological, psychological and ethical effects of these disorders on individuals and society. Modern approaches such as genetic counseling, prenatal diagnostic techniques, personalized medicine and gene therapy are also important components of the course. In this way, students gain the ability to evaluate genetic diseases from a holistic perspective.

Course Category
Mathematics and Basic Sciences %0
Engineering %0
Engineering Design %0
Social Sciences %0
Education %0
Science %100
Health %0
Field %0

Planned Learning Activities and Teaching Methods
Activities are given in detail in the section of "Assessment Methods and Criteria" and "Workload Calculation"

Assessment Methods and Criteria
Veri yok

 
ECTS Allocated Based on Student Workload
Activities Quantity Duration Total Work Load
Yazılı Sınav 1 2 2
F2F Dersi 13 3 39
Grup Sunumu 1 1 1
Ev Ödevi 1 4 4
Sınıf İçi Aktivitesi 13 1 13
Sunum 1 3 3
Okuma 10 2 20
Tekrar Anlatım 1 3 3
Yüz Yüze Ders 13 3 39
Derse Devam 10 3 30
Final Sınavı 1 2 2
Total Work Load   Number of ECTS Credits 5 156

Course Learning Outcomes: Upon the successful completion of this course, students will be able to:
NoLearning Outcomes
1 To provide the details of basic principles of different types of inheritance patterns of human diseases
2 To make the students familiar with the basic concepts of mendelian inheritance and multigenic inheritance of the diseases
3 To provide basic knowledge in the field of epigenetic and transgenerational inheritance
4 To give students main information behind the potential implications of personalized and genomic medicine


Weekly Detailed Course Contents
WeekTopicsStudy MaterialsMaterials
1 Introduction to genetic diseases
2 Mendelian disease I
3 Mendelian disease I - Specific examples
4 Mixed/Complex Inheritance I: Overview of complex trait inheritance, including epigenetic and environmental effects, modifiers of Mendelian disease
5 Mixed/Complex Inheritance II-Specific examples
6 Complex diseases- I: complex traits such as height and puberty
7 Complex diseases- II: Type II diabetes, obesity
8 Complex diseases- III: cancer genetics, infectious disease genetics
9 Personalized Medicine and Personal Genomics I: What are personalized medicine and personal genomics?
10 Personalized Medicine and Personal Genomics II: Ethical considerations
11 Presentations I
12 Presentations II
13 Presentations III


Contribution of Learning Outcomes to Programme Outcomes
P1 P2 P3 P4 P5 P6 P7 P8 P9 P10 P11 P12
C1 5 5 4 3 3 2 2 3 3 2
C2 5 5 3 3 2 2 3 3 3 2
C3 5 5 4 4 3 2 3 4 3 2
C4 5 5 3 4 2 2 3 3 3 2

Contribution: 1: Very Slight 2:Slight 3:Moderate 4:Significant 5:Very Significant


https://sis.agu.edu.tr/oibs/bologna/progCourseDetails.aspx?curCourse=72028&lang=en