Genetic Diagram Albinism. However this is contrary to definitions where the condition is. If the two of you do then each child has a 1 in 4 chance of having albinism.
Albinism is a congenital disorder characterized in humans by the complete or partial absence of pigment in the skin hair and eyes. Melanin also plays a role in the development of certain optical nerves so all forms of albinism cause problems with the development and function of the eyes. Albinism is a well recognized phenomenon in molluscs both in the shell and in the soft parts.
If only one or neither of you is a carrier then each child has pretty close to a zero chance for albinism.
Mutations in the oca2 gene are responsible for type 2. Albinism related to rare hereditary syndromes can. Albinism is a rare group of genetic disorders that cause the skin hair or eyes to have little or no color. Melanin also plays a role in the development of certain optical nerves so all forms of albinism cause problems with the development and function of the eyes.
