Match List-I with List-II

List-I List-II
(a) Haemophilia (i) Inborn error of metabolism which lacks an enzyme that converts phenylalanine into tyrosine
(b) Down's Syndrome (ii) Sex-linked recessive disorder; a defect in blood coagulation
(c) Phenylketonuria (iii) Presence of additional copy of X-chromosome  (44+XXY)
(d) Klinefelter's Syndrome (iv) Additional copy of chromosome number 21

Choose  the correct answer from the options given below:

(a) (b) (c) (d)
1. (ii) (iv) (i) (iii)
2. (iv) (ii) (i) (iii)
3. (ii) (iii) (i) (iv)
4 (i) (ii) (iii) (iv)
Subtopic:  Mendelian Disorders | Non - Disjunction & Aneuploidy | Sex Aneuploidy - Turner & Klinefelter Syndrome |
 88%
Level 1: 80%+
NEET - 2022
Hints

Match List-I with List-II:
List-I List-II
A.   Down's syndrome  I.  \(11^{\text {th }}\) chromosome
B.  \(\alpha\) -Thalassemia  II.  \(' \mathrm{X} '\) chromosome
C.  \(\beta\) -Thalassemia  III.  \(21^{\text {st }}\) chromosome
D.  Klinefelter's
syndrome
IV.  \(16^{\text {th }}\) chromosome

Choose the correct answer from the options given below:
1. A-II, B-III,C-IV, D-I 
2. A-III, B-IV,C-I, D-II 
3. A-IV, B-I, C-II, D-III 
4. A-I, B-II, C-III, D-IV
Subtopic:  Mendelian Disorders | Chromosomal Disorders |
 88%
Level 1: 80%+
NEET - 2024
Hints

What is not true regarding Phenylketonuria?
1. It is an inborn error of metabolism.
2. It is inherited as an autosomal recessive trait.
3. The affected individual lacks an enzyme that converts the amino acid tyrosine into phenylalanine.
4. Accumulation of phenylpyruvic acid in brain results in mental retardation.
Subtopic:  Mendelian Disorders |
 82%
Level 1: 80%+
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