Question

6. Tay-Sachs disease (TSD) is an inborn error of metabolism that results in death, usually by age two. You are a genetic coun

1 0
Add a comment Improve this question Transcribed image text
Answer #1

a) ge 엔 Борд Aa Maternal uncle Аа aa Male Female cousin b) Both male e female are unaffected. Presbability that they are carr

Please rate high.

Add a comment
Know the answer?
Add Answer to:
6. Tay-Sachs disease (TSD) is an inborn error of metabolism that results in death, usually by...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • Tay-Sachs disease (infantile amaurotic idiocy) is a rare human disease in which toxic substances ...

    Tay-Sachs disease (infantile amaurotic idiocy) is a rare human disease in which toxic substances accumulate in nerve cells. The recessive allele responsible for the disease is inherited in a simple Mendelian manner. A woman is planning to marry her first cousin (their fathers are brothers), but the couple discovers that their shared grandfather's sister died in infancy of Tay-Sachs disease and their shared great grandparents didn't have this disease. What is the probability that the cousins' first child will have...

  • 1. Tay-Sachs is an autosomal recessive disorder, which is the inability for infants to breakdown gangliosides in the CNS, which overtime build-up and destroy neurons. As the disease progresses, the ch...

    1. Tay-Sachs is an autosomal recessive disorder, which is the inability for infants to breakdown gangliosides in the CNS, which overtime build-up and destroy neurons. As the disease progresses, the child loses muscle control. Eventually, this leads to blindness, paralysis and death. If you have a family history of Tay-Sachs disease or if you're a member of a high-risk group and plan to have children, doctors strongly recommend genetic testing and genetic counseling. Scott and Tina are a young couple...

  • Use the information presented below to answer questions 6 - 8. Tay-Sachs disease is a recessive...

    Use the information presented below to answer questions 6 - 8. Tay-Sachs disease is a recessive hereditary abnormality causing death within the first few years of life in individuals with the genotype tt. These individuals never reach sexual maturity. Individuals with the genotype T do not become diseased. Abnormally shortened fingers (brachyphalangy) are due to the presence of alleles in the heterozygous condition (Bb) located at a different locus. Geneticists observed that brachyphalangy was conveyed by the dominant allele and...

  • not sure if i did this right. please help. 1. Phenylketonuria (PKU) is a human metabolic...

    not sure if i did this right. please help. 1. Phenylketonuria (PKU) is a human metabolic disorder in whic allele a, lack a liver enzyme required for the breakdown of excess phens intellectual disabilities, delayed development, behavioral an problems. Men and women have an equal chance of inher (her father's father) with PKU. Jessica is married to a man nam has two phenotypically unaffected parents but he has a brothe Jessica's paternal grandmother and both maternal grandpare members mentioned, and...

  • Styles 6. Insert a picture of your pedigree chart for this family with genotypes filled in...

    Styles 6. Insert a picture of your pedigree chart for this family with genotypes filled in here. 7. Which pattern of inheritance do you think the disease shows? Explain your reasoning. 8. Patient 1 and Patient 2 in the pedigree chart would like to know what the chances are that they will have a child with the disease. What do you tell them? Use a Punnett Square to show your work. Using Punnett Squares for human conditions and diseases The...

  • Creating a pedigree chart from a family history and hypothesizing pattern of inheritance A family with...

    Creating a pedigree chart from a family history and hypothesizing pattern of inheritance A family with a new disease caused by a mutant gene has been found. The family history has been collected and recorded. You will now create a pedigree chart from their family history and use the pedigree to predict the pattern of inheritance the disease follows. • Read the following family history: Patient 1 and Patient 2 visited a genetics counselor and provided their family histories. As...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT