Column I
(i) Sickle-cell anaemia
(ii) Alkeptonuria
(iii) Albinism
(iv) Phenylketonuria
Column II
(a) Homogentisic acid
(b) Lack of melanin
(c) Accumulation of amino acid
(d) Defective haemoglobin
Answers
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Hy,
1. Sickle cell anaemia- d. Defective of haemoglobin
2. Alkeptonutia- a. Homogenestic acid
3. Albinism- b. Lack of melanin
4. Phenylketonuria - c. Accumulation of amino acid
Hope it helps
Regards
Dr Chinmay
Thanks
1. Sickle cell anaemia- d. Defective of haemoglobin
2. Alkeptonutia- a. Homogenestic acid
3. Albinism- b. Lack of melanin
4. Phenylketonuria - c. Accumulation of amino acid
Hope it helps
Regards
Dr Chinmay
Thanks
Answered by
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Dear Student,
◆ Answer -
Diseases in column I are matched with their descriptions in column II as the following -
(i) Sickle-cell anaemia - (d) Defective haemoglobin
- Sickle cell hemoglobin (HbS) is present.
(ii) Alkeptonuria - (a) Homogentisic acid
- Deficiency of homogentisate oxygenase
(iii) Albinism - (b) Lack of melanin
- Skin darkening pigment melanin is absent.
(iv) Phenylketonuria - (c) Accumulation of amino acid
- Build up of phenylalanine in the the body.
Thanks dear for asking. Hope this helps you...
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