In: Biology
Q) The woman is planning to marry her first cousin , but they discovers that their shared grandfather's sister died in infancy due to Tay-Sach's disease (a rare autosomal recessive disorder).
Draw the relevant parts of the pedigree as described, and show all genotypes.
Answer:- Tay-sach's disease is an autosomal recessive disorder, in autosomal recessive disorder traits appear equally in males and females, if parents are healthy carriers than 25% of children gets affected.
in the above chart as per question The woman who is planning to marry her first cousin, discovers that their shared grandfather's sister is affected by Tay-sach's disease, so in
Generation-1 , Grand fathers parents were both carriers of the disease (Tt * Tt)
Generation-2 they gave rise to four children 1 normal female, 1 carrier male, 1 affected female and 1 carrier male.
In Generation-2, carrier male (Women's shared grandfather )married to a normal female (Tt * TT)
In Generation-3 they had 4 children 1 is normal male, 1 carrier female, 1 normal male , 1 carrier female.
In Generation-3 carrier female got married to a normal male (Tt * TT)
In Generation-4 they gave rise to 1 normal female , 1 carrier male, 1 normal female, 1 carrier male.
and in Generation-3, the mating between a normal male and normal female (TT * TT) gave rise to Normal childs.
In Generation -4 when IV- 3 married with IV - 4 , here both are normal male and female .(TT * TT)
So in Genartion -5 all the child's will be normal ,
so the chance of cousin's first child having Tay-sach's disease is 0% , it will be a normal child.
as all the people who marry into the family are homozygous normal.