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Direction: Read the following text and answer the following questions on the basis of the same :
Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.
It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :
— Both parents have sickle cell trait
— One parent has sickle cell anaemia and the other has sickle cell trait
— Both parents have sickle cell anaemia
If both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.
  • a)
    25 % risk
  • b)
    50 % risk
  • c)
    75% risk
  • d)
    No risk
Correct answer is option 'B'. Can you explain this answer?
Verified Answer
Direction: Read the following text and answer the following questions...
If both parents have sickle cell trait, there is a 50% chance with each pregnancy that the baby will have sickle cell trait. A child with sickle cell anemia appears normal at birth.
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Most Upvoted Answer
Direction: Read the following text and answer the following questions...
Explanation:

Risk of the child having sickle cell trait:
- When both parents have sickle cell trait, each parent contributes one copy of the defective gene.
- The child has a 50% chance of inheriting the defective gene from each parent.
- The Punnett square predicts that there is a 25% chance of the child inheriting two normal genes, a 50% chance of inheriting one normal and one defective gene (sickle cell trait), and a 25% chance of inheriting two defective genes (sickle cell anaemia).
- Therefore, there is a 50% risk of the child having sickle cell trait when both parents have sickle cell trait.
Therefore, the correct answer is option B) 50% risk.
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Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer?
Question Description
Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer? for NEET 2024 is part of NEET preparation. The Question and answers have been prepared according to the NEET exam syllabus. Information about Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer? covers all topics & solutions for NEET 2024 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer?.
Solutions for Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer? in English & in Hindi are available as part of our courses for NEET. Download more important topics, notes, lectures and mock test series for NEET Exam by signing up for free.
Here you can find the meaning of Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer? defined & explained in the simplest way possible. Besides giving the explanation of Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer?, a detailed solution for Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer? has been provided alongside types of Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer? theory, EduRev gives you an ample number of questions to practice Direction: Read the following text and answer the following questions on the basis of the same :Sickle cell anaemia is a genetic disorder where the body produces an abnormal haemoglobin called haemoglobins. Red blood cells are normally flexible and round, but when the haemoglobin is defective, blood cells take on a “sickle” or crescent shape. Sickle cell anaemia is caused by mutations in a gene called HBB.It is an inherited blood disorder that occurs if both the maternal and paternal copies of the HBB gene are defective. In other words, if an individual receives just one copy of the defective HBB gene, either from mother or father, then the individual has no sickle cell anaemia but has what is called “sickle cell trait”. People with sickle cell trait usually do not have any symptoms or problems but they can pass the mutated gene onto their children. Three inheritance scenarios can lead to a child having sickle cell anaemia :— Both parents have sickle cell trait— One parent has sickle cell anaemia and the other has sickle cell trait— Both parents have sickle cell anaemiaIf both parents have sickle cell trait, then there is _______________of the child having sickle cell trait.a)25 % riskb)50 % riskc)75% riskd)No riskCorrect answer is option 'B'. Can you explain this answer? tests, examples and also practice NEET tests.
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