Science, asked by Anonymous, 8 months ago

Write about hereditary colour blindness

Answers

Answered by DivyanshJoshi07
1

Answer:

when mother gene or father gene has difficult in seeing colours there exist the deficiency of vitamin A which comes as heredity in the child

Answered by Anonymous
1

Hi mate,

here's the answer

Different kinds of colour-blindness have been detected but in the most common

Again this is due to the presence of a defective gene or absence of the gene,responsible for colour vision.The genes for both haemophilia and colour-blindness are located on X-chromosome,

and hence, the disorder is passed down from mother to the son because a boy receives the X chromosome from the mother and Y chromosome from the father.

In the mother, with two X-chromosomes, the defect does not show up. Also in the

daughter, the effect of defective gene on X-chromosome inherited from mother

may be masked by a normal gene on the X-chromosome, inherited from her father.

Since X chromosome bears the defective gene,

the son suffers from the genetic disorder, as male has only one X chromosome and one Y chromosome and so the defective gene does not get masked.

hope this helps you

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