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How can someone cope with a child with colorblindness?

Updated: 8/18/2019
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Q: How can someone cope with a child with colorblindness?
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Is their a cure for colorblindness?

Colorblindness is usually a genetic trait. There is no more a cure for genetic colorblindness than there is for blond hair.


Does race affect colorblindness?

No you must not choose any diverse colorblindness


What is the proper name for colorblindness?

The proper name for colorblindness is color vision deficiency.


Which parental pair could produce females with colorblindness?

Yes. Two normal-visioned parents can produce a color blind child only if both the parents have are heterozygous. To determine the phenotypes of the parents, you will have to look at their parents.


What can be done to cure colorblindness?

As of 2016 there is no cure or treatment for colorblindness.


Snice the allele for colorblindness is located on the x chromosome which type of trait is colorblindness?

Sex linked


What does monochromatic?

a monochromat is someone who is color blind. It is the rarest form of colorblindness, true monochromats only see shades of light and dark


Is a carrier for colorblindness is colorblind?

Not necessarily. The allele for colorblindness is recessive. For a female, in order to be colorblind she must have to recessive alleles for colorblindness. Example: XcXc would be colorblind. XCXc would be a carrier for colorblindness, but not colorblind. For a male, because colorblindness is a sex-linked gene, he only needs one allele to be colorblind. Example: XcY is colorblind. XCY is not colorblind.


How do you cope if you cheated on someone?

fess up. And don't do it again.


If a color blind male who has normal clotting blood marries a female who is a carrier of hemophilia and has normal color vision could they have a color blind child?

In short, hemophilia has nothing to do with colorblindness, but YES, they could have a colorblind child if she is a carrier for the colorblindness gene. Color blindness is an X-linked trait. That means it is carried in the X chromosome, which differentiates whether a baby will be a girl or a boy. Women have two X chromosomes (XX), and men have an XY combination. If a woman is a carrier for color blindness, only one of her chromosomes will be affected (we'll call it a little "x"), and for that reason she will not be colorblind. Men, on the other hand, only have one X chromosome, so any time they carry the colorblindness gene, they will be colorblind. A woman will carry the colorblindness gene if: a. Her father is colorblind b. Any of her offpsring are colorblind She may carry the colorblindness gene if: a. Male family members (brothers, uncles, etc.) are colorblind A child inherits one chromosome from each parent. He/She will get an X chromosome from his/her mother, and an X from her father (if a girl) or a Y from his father (if a boy). So, If a woman has normal vision (assuming she does not have a family history of colorblindness), XX, and a man is colorblind, xY, they have several different chances for different offspring: Xx (a normal girl who carries the colorblindness gene) XY (a normal boy) Xx (a normal girl who carries the colorblindness gene) XY (a normal boy) The short answer is that ALL CHILDREN WILL HAVE NORMAL VISION. However, all daughters will be CARRIERS, meaning they can pass colorblindness on to their children.