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).
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.
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.
An Autosomal recessive pattern is one in which certain genes of the X sex chromosome are turned off, autosomal is in reference to the X chromosome and the fact that the genes are turned off is indicated by the recessive. So in the case of Albinism the pigmentation genes in the X chromosome are turned off causing the various side effects.
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.