no albinism is a genetic disorders that changes an offsprings physical appearance from its original parents. it may also bring out the offsprings recessive traits. its also a cause of mental retardation
yes it is. It affects chromosome 11.
Chromosome 9.
*affected
Albinism is a congenital disorder.
Chromosome Disorder
Chromosome 9.
Down syndrome is a chromosomal disorder. It is caused by having 1 extra chromosome (chromosome 21).
Albinism is a genetic disorder in which pigment in the skin and/or eyes is absent or reduced. It is not a movement or religion (-ism).
Sex-linked disorders are passed on the X chromosome. The man supplies the Y chromosome to his sons so the disorder cannot be passed on to the sons. But the man gives his daughter an X chromosome so the disorder can be passed on to her.
Ocular albinism (OA1) is caused by a genetic defect on chromosome 11 of the GPR143 gene. Oculocutaneous albinism type 2 (OCA2 or P gene albinism) results from a genetic defect on chromosome 15 in the P protein that helps the tyrosinase enzyme to function. Oculocutaneous albinism type 3 (OCA3) is rarely described and results from a genetic defect on chromosome 9 in TYRP1, a protein related to tyrosinase. Oculocutaneous albinism type 4 (OCA4) results from a genetic defect in chromosome 5 at position 13.3, in the SLC45A2 protein that helps the tyrosinase enzyme to function.
If both parents carry the gene for albinism, which is an autosomal recessive disorder, there is a 25% chance their child will be affected by albinism, a 50% chance the child will be a carrier like the parents, and a 25% chance the child will neither have albinism nor be a carrier. Therefore, there is a 75% chance that their child will not have albinism, either being a carrier or completely unaffected.
Yes. If either parent is a carrier of the gene that causes albinism then their child becomes a carrier as well. It is only when both parents have the gene for albinism that the child is born with this disorder.