Sickle cell anaemia results from.

1. A chromosomal aberration

2. Non disjunction of autosome

3. A point mutation

4. Blood transfusion reaction

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 80%
Level 1: 80%+
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Identify the incorrect statement:

(1) In addition to recombination, mutation is another phenomeonon that leads to variation in DNA.

(2) Chromosomal aberrations are commonly observed in cancer cells.

(3) A classical example of a point mutation is sickle cell anaemia.

(4) Non ionising radiations cannot be mutations. 

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 77%
Level 2: 60%+
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Given below is the initial amino acids of the beta chain of a hemoglobin molecule. What will be true about this hemoglobin molecule ?

1. The RBCs carrying this molecule will undergo sickling at high oxygen tension
2. The RBCs carrying this molecules will undergo sickling at low oxygen tension
3. There will be a quantitative decrease in the synthesis of this molecule
4. This is normal beta chain of the hemoglobin molecule
Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 53%
Level 3: 35%-60%
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Sickel cell anaemia is

(1) an autosomal linked dominant trait 

(2) caused by substitution of valine by glutamic acid in the β-globin chain of haemoglobin.

(3) caused by a change in base pair of DNA

(4) characterized by elongated sickle like RBCs with a nucleus. 

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
Level 3: 35%-60%
NEET - 2009
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Sickle cell anaemia has not been eliminated from the African population because :

(1) it is controlled by recessive genes

(b) it is not a fatal disease

(3) it provides immunity against malaria

(4) it is controlled by a dominant genes

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 66%
Level 2: 60%+
NEET - 2006
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Sickle cell anaemia is example of 

(1) sex-linked inheritance

(2) deficiency disease

(3) autosomal heritable disease

(4) infectious disease

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 81%
Level 1: 80%+
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Sickle cell anaemia is a classic example of

(1) Point mutation

(2) silent mutation

(3) Frame shift mutation

(4) non sense mutation

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 92%
Level 1: 80%+
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If a normal female has a sickle cell anaemic child what can be the probable genotype of that gene in that female?

(1) AA

(2) aa

(3) Aa

(4) both (1) and (3)

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 65%
Level 2: 60%+
Hints

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Which of the following disorder can’t be transmitted from a single diseased parent? 

(1) Sickle cell anaemia

(2) Haemophilia

(3) Colour Blindness

(4) Myotonic dystrophy

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 57%
Level 3: 35%-60%
Hints

Which of the following genotypes could cause Sickle cell anaemia? 

1. Hbˢ + Hbᴬ

2. Hbᴬ+ Hbᴬ

3. Hbˢ + Hbˢ

4. Both ‘A’ and ‘C’.

Subtopic:  Mendelian Disorders: Sickle Cell Anemia |
 74%
Level 2: 60%+
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