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Examination Methods in Medical Genetics

Class at Second Faculty of Medicine |
D01000107

Syllabus

Syllabus - Examination Methods in Medical Genetics

Topics:

Brief overview of formal genetics and cytogenetics - genome and phenome, genotype and phenotype, chromosomes and chromosomal aberrations

Introduction to medical genetics, key discoveries and milestones of medical genetics; medical genetics in the post-genomic era

Genetic counseling unit, its basic activities and cooperation with other clinical departments, ethical and legal issues of genetic counseling, current problems of medical genetics - seminar with a physician - specialist in genetic counseling

From symptoms to syndromes - how to examine a patient and indicate cytogenetic or molecular genetic examination; interesting case studies in medical genetics

Medical genetic lab, its equipment, the most serious health hazards

Diagnostic tools and basic techniques in medical cytogenetics, banding methods, karyotyping

Modern molecular cytogenetic methods (FISH, MLPA, arrayCGH), their application in clinical genetics

Mosaic findings in clinical genetics - their consequences, diagnostic possibilities and limitations, and interpretation problems (e.g. on mosaic forms of Turner's syndrome)

Examination methods in oncogenetics and oncocytogenetics

The most important information sources in medical genetics and cytogenetics

How to publish scientific reports in medical genetics

Practical activities:

Observation and determination of human chromosomes

Seeing a molecular cytogenetic lab - demonstration of fluorescent microscope

Demonstration of the basic FISH and M-FISH analysis