Advertisements
Advertisements
Question
About 8% of the human male population suffers from colour blindness, whereas only about 0.4% of the human female population suffers from this disease. Write an explanation to show how it is possible.
Advertisements
Solution
Colour blindness is a sex-linked disorder and is caused by a recessive gene located on the X chromosome. The Y chromosome of male does not carry any gene for colour vision and the defect appears in the presence of a single recessive gene (XcY). As a result, colour blindness is more common in males (8%) as compared to females (0.4%).
RELATED QUESTIONS
Identify ‘a’, ‘b’, ‘c’, ‘d’, ‘e’ and ‘f’ in the table given below:
| S. No. | Syndrome | Cause | Characteristics of affected individuals | Sex (male/female/both) |
| 1. | Down’s | Trisomy of 21 |
‘a’ |
‘b’ |
| 2. | ‘c’ | XXY | Overall masculine development | ‘d’ |
| 3. | Turner’s | 45 with XO |
‘e’ |
‘f’ |
State any two symptoms of Down’s syndrome.
Identify the genetic disorder m which an individual has an overall masculine development, gynaecomastia and is sterile.
Following list indicates various genetic diseases. Identify the diseases that are not caused due to single gene defect.
Huntington's chorea, alkaptonuria, Sickle cell anaemia, Down syndrome, thalassemia, Taysachs disease, Turner syndrome, cystic fibrosis, haemophi Lia, Klinefelter syndrome, albinism
A short stature with webbing of neck and low posterior hairline indicates ______ syndrome.
HbA and HbS alleles of normal and sickle celled RBC are ______.
If a colour-blind man marries a woman who is homozygous for normal colour vision, the probability of their son being colour-blind is ______.
The most striking example of point mutation is found in a disease called ______.
Placed below is a karyotype of a human being.

On the basis of this karyotype, which of the following conclusions can be drawn: ______
The practice of analyzing inheritance patterns in human beings is called ______
