Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
19. Cancer Genetics
Overview of Cancer
4:04 minutes
Problem 11d
Textbook Question
Textbook QuestionGo to the website http://www.ncbi.nlm.nih.gov/omim and enter 'Lynch syndrome' in the Search box at the top of the page. From the list of options given, select '#120435—Lynch Syndrome.' Use the information you retrieve to answer the following questions. There are two types of Lynch syndrome. What are they?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Lynch Syndrome
Lynch syndrome, also known as hereditary nonpolyposis colorectal cancer (HNPCC), is a genetic condition that increases the risk of various cancers, particularly colorectal and endometrial cancers. It is caused by inherited mutations in mismatch repair (MMR) genes, which are responsible for correcting DNA replication errors. Understanding Lynch syndrome is crucial for identifying affected individuals and implementing appropriate screening and preventive measures.
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Types of Lynch Syndrome
There are two main types of Lynch syndrome: Lynch syndrome type I, which primarily increases the risk of colorectal cancer, and Lynch syndrome type II, which is associated with a broader spectrum of cancers, including endometrial, ovarian, gastric, and urinary tract cancers. Recognizing these types helps in tailoring surveillance strategies and genetic counseling for affected families.
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Genetic Testing and Counseling
Genetic testing for Lynch syndrome involves analyzing specific MMR genes to identify mutations that predispose individuals to cancer. Genetic counseling is essential for individuals with a family history of Lynch syndrome, as it provides information about risks, testing options, and preventive measures. This process aids in informed decision-making regarding health management and family planning.
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