Question on: JAMB Biology - 2019
Albinism is an expression of trait controlled by
Chromosomes
Recessive genes
Dominant genes
Mutation
Albinism is a congenital disorder characterized in humans by the complete or partial absence of pigment in the skin, hair and eyes. Albinism is associated with a number of vision defects, such as photophobia, nystagmus, and amblyopia. Lack of skin pigmentation makes for more susceptibility to sunburn and skin cancers.
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