Autosomal recessive traits
- Appear with equal frequency in males and females.
- Appear when a person inherits two alleles for a trait, one from each parent.
- When both parents are heterozygotes, ¼ of the offspring express the trait.
- Appear more in consanguinious couples.
- Affected children are commonly born to unaffected parents (carrier)
- Tend to skip generation
- E.g., tay-sach
Autosomal dominant trait
- Doesn't skip generation
- Appear equally in both sexes
- Affected child has an affected parent
- If one parent is heterozygous for the trait and other is unaffected, ½ of the offspring will be affected.
- E.g., familial hypercholesterolemia
X-linked recessive trait
- Appear more frequently in males than female
- Affected males are born to unaffected mother
- Tend to skip generation
- Heterozygous mother gives ½ sons affected and ½ daughter as unaffected carriers.
- Not passed from father to son
- E.g. hemophilia A
X-linked dominant trait
- Appear equal in male and female but affect more female than male
- Must affected parents
- Do not skip generation
- Affected father pass trait to all daughters and none of the son.
- Affected mother pass to ½ sons and ½ daughters.
- E.g hypophosphatemia I or familial vitamin D resistant rickets.
Y-linked traits
- Only males are affected
- Trait is passed from father to son .
- Does not skip generation
- E.g. maleness
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