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प्रश्न
Suggest how pedigree analysis can be useful?
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उत्तर
- It is beneficial for genetic counsellors to advise prospective couples of the likelihood of having children with genetic disorders such as haemophilia, colour blindness, alkaptonuria, phenylketonuria, thalassemia, sickle cell anaemia (recessive traits), brachydactyly, and syndactyly (dominant traits).
- Pedigree analysis shows that Mendel's ideas are relevant to human genetics, with some later discoveries like quantitative inheritance, sex-linked traits, and other connections.
- It can suggest the genesis of a characteristic in forebears; for example, haemophilia appeared in Queen Victoria and spread throughout Europe's royal dynasties through marriage.
- It is helpful to understand the probability of a recessive allele causing a condition in the progeny, such as thalassemia, muscular dystrophy, or haemophilia.
- It can suggest the potential harm that a marriage between close relatives could cause.
- It can help determine whether a recessive or dominant gene is the cause of a genetic condition.
- In certain situations, it may be useful to identify the genotypes of unborn children.
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संबंधित प्रश्न
The pedigree chart given below shows a particular trait which is absent in parents but present in the next generatoin irrespective of sexes. Draw your conclusion on the basis of the pedigree.
A normal visioned woman, whose father is colour blind, marries a normal visioned man. What would be probability of her sons and daughters to be colour blind? Explain with the help of a pedigree chart.
Study the Pedigree chart given below and answer the questions that follow:

Symbols used in the given Pedigree Chart are as follows:
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Carrier male |
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Affected male |
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Normal male |
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Carrier female |
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Affected female |
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Normal female |
(a) On the basis of the inheritance pattern exhibited in this pedigree chart, what conclusion can you draw about the pattern of inheritance?
(b) If the female is homozygous for the affected trait in this pedigree chart, then what percentage of her sons will be affected?
(c) Give the genotype of offspring 1, 2, 3 and 4 in III generations.
OR
(c) In this type of inheritance pattern, out of male and female children which one has less probability of receiving the trait from the parents? Give a reason.
What should be the genotype of the indicated member?







