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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 anaemiaSickle cell anaemia is a/an ________________ disease.a)X linkedb)autosomal dominantc)autosomal recessived)Y linkedCorrect answer is option 'C'. Can you explain this answer? for NEET 2024 is part of NEET preparation. The Question and answers have been prepared
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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 anaemiaSickle cell anaemia is a/an ________________ disease.a)X linkedb)autosomal dominantc)autosomal recessived)Y linkedCorrect answer is option 'C'. 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 anaemiaSickle cell anaemia is a/an ________________ disease.a)X linkedb)autosomal dominantc)autosomal recessived)Y linkedCorrect answer is option 'C'. 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 anaemiaSickle cell anaemia is a/an ________________ disease.a)X linkedb)autosomal dominantc)autosomal recessived)Y linkedCorrect answer is option 'C'. Can you explain this answer? in English & in Hindi are available as part of our courses for NEET.
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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 anaemiaSickle cell anaemia is a/an ________________ disease.a)X linkedb)autosomal dominantc)autosomal recessived)Y linkedCorrect answer is option 'C'. 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 anaemiaSickle cell anaemia is a/an ________________ disease.a)X linkedb)autosomal dominantc)autosomal recessived)Y linkedCorrect answer is option 'C'. 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 anaemiaSickle cell anaemia is a/an ________________ disease.a)X linkedb)autosomal dominantc)autosomal recessived)Y linkedCorrect answer is option 'C'. 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 anaemiaSickle cell anaemia is a/an ________________ disease.a)X linkedb)autosomal dominantc)autosomal recessived)Y linkedCorrect answer is option 'C'. 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 anaemiaSickle cell anaemia is a/an ________________ disease.a)X linkedb)autosomal dominantc)autosomal recessived)Y linkedCorrect answer is option 'C'. Can you explain this answer? tests, examples and also practice NEET tests.