Question

3.Another patient has a family history in which: 1. the disease was equally distributed among the...

3.Another patient has a family history in which:

1. the disease was equally distributed among the male

and female offspring of affected females

2. all daughters of an affected male were affected

3. none of the sons of an affected male and unaffected

female were affected

What type of inheritance is this likely to be?

A. Autosomal dominant

B. Autosomal recessive

C. X-linked dominant

D. X-linked recessive

4. Another patient has a family history in which:

1. carrier females transmit the trait to half of their

sons

2. none of the carrier females daughters were

affected, but half were carriers

What type of inheritance is this likely to be?

A. Autosomal dominant

B. Autosomal recessive

C. X-linked dominant

D. X-linked recessive

5. Another patient has a family history in which:

1. males and females were equally affected

2. two of the offspring from two unaffected parents

were affected, while the other six offspring were

unaffected.

What type of inheritance is this likely to be?

A. Autosomal dominant

B. Autosomal recessive

C. X-linked dominant

D. X-linked recessive

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

3) this disease is X-linked dominant

.a) the disease was equally distributed among the male and female offspring of affected females:

both males and females inherit an X chromosome from mother, here hen mother is affected half of the sons are affected and half of the female offsprings are affected, means the female had mutation in one of the X chromosome and those offsprings which inherited mutant X chromosome ( there is equal chance to get one of these chromosomes so half of the progeny are affected and half are normal)

b) all daughters of an affected male were affected

daughters inherit one of their X chromosomes from their father if the father has dominant mutation in his X chromosome all of his daughters are affected

c) none of the sons of an affected male and unaffected

sons inherit the Y chromosome from father so sons of father having mutation in the X chromosome cannot be affected

so this is c) X-linked dominant

4) this X-linked recessive

.a) carrier females transmit the trait to half of their sons

females have 2 X-chromosomes so if they have a recessive mutation in one of their X chromosome females are not affected but they pass the affected chromosome to their sons

b) none of the carrier females daughters were affected, but half were carriers

females inherit one of their X chromosomes from father if the father is normal then all of his daughters will have normal X chromosome but half of them can inherit the affected chromosome from their mother, so half of them are carriers

so the answer is D) X-linked recessive

Add a comment
Know the answer?
Add Answer to:
3.Another patient has a family history in which: 1. the disease was equally distributed among the...
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
  • 5. Another patient has a family history in which: 1. males and females were equally affected...

    5. Another patient has a family history in which: 1. males and females were equally affected 2. two of the offspring from two unaffected parents were affected, while the other six offspring were unaffected. What type of inheritance is this likely to be? A. Autosomal dominant B. Autosomal recessive C. X-linked dominant D. X-linked recessive

  • Look carefully at the pedigrees below and: 1) indicate whether the transmission appears autosomal or sex-linked...

    Look carefully at the pedigrees below and: 1) indicate whether the transmission appears autosomal or sex-linked 2) indicate whether the transmission appears dominant or recessive 3) provide at least two characteristics for each that support your conclusion. In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at...

  • In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance:...

    In general, the following characteristics suggest (but do not prove) specific inheritance patterns: Autosomal recessive inheritance: -affected individuals can be born to unaffected parents -if both parents are affected, all children are affected -observable effect of relatedness (consanguinity) -horizontal" inheritance: trait appears at once among several members of one generation (siblings) *** Autosomal dominant inheritance each affected individual has an affected parent -when one parent is affected, transmission to the offspring (on average) *** -two unaffected parents do not transmit...

  • Hello, please please help me with this, I would greatly appreciate it!!!! THANK YOU SO MUCH!!!...

    Hello, please please help me with this, I would greatly appreciate it!!!! THANK YOU SO MUCH!!! QUESTION 3 When first presented with a pedigree, you should initially look for general trends. For example: Are there affected individuals in each generation? Are both males and females equally affected? Are traits from a father or mother passed on to all their children? Or only to their sons or daughters? Based on these general observations, you can usually make a fairly reasonable guess...

  • Part B Determining genotypes in pedigrees of X-linked conditions The pedigree from Part A is shown...

    Part B Determining genotypes in pedigrees of X-linked conditions The pedigree from Part A is shown below. Fill in the most likely genotypes of the indicated individuals in the pedigree. Note that a dominant allele followed by an underscore (_) indicates that either the dominant or the recessive allele may be present at the second position. Drag one pink label (for condition A, autosomal recessive) to each pink target. Drag one blue label (for condition B, X-linked recessive) to each...

  • Question 3 The following human pedigree shows a family affected by a specific disease. Assume that...

    Question 3 The following human pedigree shows a family affected by a specific disease. Assume that the individuals marked with an asterisk () do not carry any allele associated with the affected phenotype and that no other mutation spontaneously occurs. Also assume complete penetrance a) State the most likely mode of inheritance for this disease. Choose from: autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive b) Write all possible genotypes of the following individuals in the pedigree. Use the uppercase...

  • 모모모 < 모 2 1 | 미모 모 오 or lo III = - - genetic...

    모모모 < 모 2 1 | 미모 모 오 or lo III = - - genetic disorder is segregating. 3. Each of the pedigrees shown represents a human family within which a genetic disorder is se Assume the two traits are extremely rare in the population and completely penetrant. Part 1. For the first pedigree. lisorder: autosomal recessive, autosomal a. Determine the most probable inheritance pattern of the disorder: autosomal recessive dominant, X-linked recessive or X-linked dominant. b. Indicate the...

  • Background Problem N° 4 Objective: To use pedigrees in a case of an inherited disease in...

    Background Problem N° 4 Objective: To use pedigrees in a case of an inherited disease in humans in order to determine the type of generic inheritance 3 4 According to the National Cancer Institute (NCI), "a pedigree is an illustration of family history and it shows relationships between family members and patterns of inheritance for certain traits and diseases."3 3 2 3 Pedigrees use standard symbols and conventions: O female: male; affected | Analyze the pedigree for myopia (nearsightedness) in...

  • 12. What is a suspected heterozygous individual crossed with in a test cross? A. Homozygous dominant...

    12. What is a suspected heterozygous individual crossed with in a test cross? A. Homozygous dominant B. Homozygous recessive C. Heterozygous dominant D. Heterozygous recessive 13. Which of the following genotypes is possible in the offspring of a homozygous male with blood group A and a female with blood group B? The answers are 12B, 13B, 14C can you explain how? Α. ΙΑΙΑ 14. What type of inheritance is shown in this pedigree chart? Key: Affected O Carrier A. X-linked...

  • A B C D 1. Consider the pedigree below where affected individuals are in dark blue...

    A B C D 1. Consider the pedigree below where affected individuals are in dark blue and carriers are in lightblue._-ig.^ 3 4 5 A. (1 pts) Select the mode of inheritance shown in this pedigree and explain your reasoning: Autosomal dominant Autosomal recessive X-linked Y-linked B. (1 pts) Predict whether each of the great-grandparents (labeled A-D) are affected, carriers, or unaffected noncarriers and explain your reasoning 2. In Jabberwocks, flame eyes (F) are dominant to blue eyes ( and...

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