Everyone will get catract blindness in old age
you cannot cure Colour blindness is hereditary, it's in your genes.
yes, although not all the persons who have the color blindness 'genes' actually suffer its effects. they can be just carriers, who pass on the genes to the next generation. fyi: mostly males are affected by color blindness
A deletion in the X chromosome can result in blindness if it affects genes that are essential for vision. Genes involved in eye development and function are located on the X chromosome, so a deletion can disrupt the production of proteins necessary for normal vision. This disruption can lead to vision problems or blindness depending on the extent of the deletion and which specific genes are affected.
Color blindness is carried on male genes only.
Color blindness is typically caused by a genetic mutation affecting the genes responsible for color vision, such as the OPN1LW and OPN1MW genes on the X chromosome. It is not usually associated with translocation or deletion of genetic material.
No. It is usually a genetic disease that is caused by the genes which were inherited.
The sex linked genes cause genetic disorders on the basis of gender. For example color blindness is human is located on the X chromosome and is reflected in males more frequently.
The sex linked genes cause genetic disorders on the basis of gender. For example color blindness is human is located on the X chromosome and is reflected in males more frequently.
It means genes are in sex chromosomes. Sex genes are related
The genes that produce photopigments are carried on the X chromosome; if some of these genes are missing or damaged, color blindness will be expressed in males with a higher probability than in females because males only have one X chromosome (in females, a good gene on only one of the two X chromosomes is enough to yield the needed photopigments).
If someone is blinded due to an accident or environmental factor, this will not change her genetic information in such a way that her children are more likely to be born blind or with an increased risk of blindness.
Individuals with color blindness often have a normal male karyotype (46,XY) or female karyotype (46,XX). The genetic basis for color blindness typically involves mutations in genes located on the X chromosome, leading to different types of color vision deficiencies.