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प्रश्न
A child suffering from Thalassemia is born to a normal couple. But the mother is being blamed by the family for delivering a sick baby.
- What is Thalassemia?
- How would you counsel the family not to blame the mother for delivering a child suffering from this disease? Explain.
- List the values your counselling can propagate in the families.
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उत्तर
- Thalassemia is a group of autosomal recessive blood disorders characterized by severe anemia as a result of production of faulty haemoglobin chains. Mutations in the genes coding for the alpha, beta or delta chains constituting haemoglobin lead to the synthesis of improperly folded haemoglobin that is incapable of transporting oxygen efficiently.
- Thalassemia is an autosomal recessive disease, which means the mutation is carried on one of the autosomes, so the carrier can be any one of the two parents. It has an equal probability of coming from the mother or the father, so to just blame the mother for the child’s abnormality is unjustified.
- The values counseling can propagate in the families are:
- Give a healthy diet plan to the child.
- Accepting their child with all his/her positives and negatives.
- Neither of the parents is responsible for giving birth to a sick baby.
- The defect is caused by a random change in the genes of the child.
- Encouraging the child to follow his/her treatment regularly and lead a happy and normal life.
- Support the child emotionally by talking about fear, anxiety, and depression or stress the child feels.
संबंधित प्रश्न
Give the genotype of Turner’s syndrome.
Given below is the representation of amino acid composition not the relevant translated portion of β-chain of haemoglobin, related to the shape of human red blood cells

(a) Is this representation indicating a normal human or a sufferer from certain related genetic disease? Give reason in support of your answer.
(b) What difference would be noticed in the phenotype of the normal and the sufferer related to this gene?
(c) Who are likely to suffer more from the defect related to the gene represented the males, the females or both males and females equally? And why?
Attempt any TWO of the following:
‘The gene for sickle cell anaemia in homozygous condition is lethal and produces sickle cell trait in heterozygous carrier’. Explain.
In Klinefelter syndrome, an extra chromosome is a result of non-disjunction of X-chromosome during ____________.
Genes for cytoplasmic male sterility in plants are generally located in ______.
Mongolism is a genetic disorder which is caused by the presence of an extra chromosome number ______.
Which of the following is called as Royal disease?
At what level does the defect occur in Mendelian disorders?
Which diagnostic method is used to detect Mendelian disorders?
Which list contains only Mendelian disorders?
