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
2. Mendel's Laws of Inheritance
Probability and Genetics
2:03 minutes
Problem 25c
Textbook Question
Textbook QuestionA 'wrongful birth' case was recently brought before a court in which a child with Smith–Lemli–Opitz syndrome was born to apparently healthy parents. This syndrome is characterized by a cluster of birth defects including cleft palate, and an array of problems with the reproductive and urinary organs. Originally considered by their physician as having a nongenetic basis, the parents decided to have another child, who was also born with Smith–Lemli–Opitz syndrome. In the role of a genetic counselor, instruct the court about what occurred, including the probability of the parents having two affected offspring, knowing that the disorder is inherited as a recessive trait. Calculate the probability that both the male and female are carriers for TSD.
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Recessive Inheritance
Recessive inheritance refers to a pattern where a trait or disorder manifests only when an individual has two copies of the recessive allele, one inherited from each parent. In the case of Smith–Lemli–Opitz syndrome, both parents must be carriers of the recessive allele for their child to express the condition. If both parents are carriers, there is a 25% chance with each pregnancy that the child will inherit the disorder.
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Carrier Probability
Carrier probability is the likelihood that an individual possesses one copy of a recessive allele without showing symptoms of the associated disorder. In genetic counseling, determining the carrier status of parents is crucial, especially when a recessive condition is involved. If one child is affected, the probability that both parents are carriers increases, which can be calculated using Punnett squares or probability formulas.
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Smith–Lemli–Opitz Syndrome
Smith–Lemli–Opitz syndrome is a genetic disorder caused by a deficiency in the enzyme 7-dehydrocholesterol reductase, leading to abnormal cholesterol synthesis. This syndrome is characterized by a range of physical and developmental issues, including cleft palate and organ malformations. Understanding the genetic basis and inheritance pattern of this syndrome is essential for genetic counseling and assessing the risk of recurrence in future pregnancies.
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