A man and a woman affected with Babomania mate and have an unaffected daughter. Which of the following mechanisms of inheritance can be ruled out?
Choose all that can be ruled out.
Autosomal Recessive
Autosomal Dominant
Answer- Autosomal recessive
Considering, 'A' is dominant allele and 'a' is recessive allele
Lets take 2 cases :
Case 1: Disease is autosomal recessive
This means that genotype of both the parents will be 'aa'. And the cross between 'aa' genotypes will produce progeny with only 'aa' I.e. diseased phenotype. Refer punnette's cross below:
| a | a | |
| a | aa | aa |
| a | aa | aa |
Case 2: Disease is autosomal dominant
Genotype of parent 1: AA or Aa
Genotype of parent 2: Aa or AA
Now, since the progeny is disease free that means the genotype has to be 'aa'. Now from the above possibilities it can be seen that it is possible with only 1 genotype combination of both parents: Aa X Aa. Only this type of cross will produce 'aa' genotype I.e. normal phenotype. Refer punnette's cross below:
| A | a | |
| A | AA | Aa |
| a | Aa | aa |
So concluding it, the progeny being disease free but both parents showing disease is only possible when the disease is autosomal dominant. Thus we can rule out autosomal recessive possibility.
A man and a woman affected with Babomania mate and have an unaffected daughter. Which of...
A man with a specific unusual genetic trait (leading to
heterozygosity) is
house with an unaffected and non-carrying woman, and they have four
children. The pedigrees of
this family is shown in graphs a-e. For each inheritance mode
indicate
how many children of each sex will express the trait (color those
affected in each tree
genealogical according to the type of inheritance).
a) Autosomal recessive trait:
b) Autosomal dominant trait:
c) X-linked recessive trait:
d) X-linked dominant trait:
e) Trait...
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1. (20 points) a. The short pedigree below shows affected individuals in this family in red. Which modes of inheritance (X-linked recessive, X-linked dominant, Y-linked, autosomal recessive, autosomal dominant) can be ruled out, and which mode is most likely? b. (10 points) What is the likelihood that child A will be affected? Child B? O ■ ● Co
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...
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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...
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