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
6. Chromosomal Variation
Chromosomal Mutations: Aneuploidy
4:12 minutes
Problem 27c
Textbook Question
Textbook QuestionA boy with Klinefelter syndrome (47,XXY) is born to a mother who is phenotypically normal and a father who has the X-linked skin condition called anhidrotic ectodermal dysplasia. The mother's skin is completely normal with no signs of the skin abnormality. In contrast, her son has patches of normal skin and patches of abnormal skin. Which parent contributed the abnormal gamete?
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Klinefelter Syndrome
Klinefelter syndrome is a genetic condition in males characterized by the presence of an extra X chromosome, resulting in a 47,XXY karyotype. This condition can lead to various physical and developmental features, including infertility, reduced testosterone levels, and sometimes learning difficulties. Understanding Klinefelter syndrome is crucial for analyzing the genetic contributions to the boy's phenotype.
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Human Sex Chromosomes
X-linked Inheritance
X-linked inheritance refers to the pattern of inheritance for genes located on the X chromosome. Conditions that are X-linked, such as anhidrotic ectodermal dysplasia, typically manifest in males who have only one X chromosome. In this case, the father, being affected by an X-linked condition, can only pass his Y chromosome to his sons, meaning the abnormal gamete must come from the mother.
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X-Inactivation
Gametogenesis and Genetic Contribution
Gametogenesis is the process by which gametes (sperm and eggs) are produced, and it plays a critical role in genetic inheritance. Each parent contributes one gamete to the offspring, determining the genetic makeup. In this scenario, since the father has an X-linked condition and the mother is phenotypically normal, the abnormal gamete that led to the son's condition must have originated from the mother, who could be a carrier of the abnormal gene.
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Descriptive Genetics
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