The parents have normal sex chromosome genotypes, XX and XY. The chromosomal error that causes Klinefelter's syndrome occurs during the formation of either of the parent's gametes during meiosis.
The children could have AO, BO, AB, or OO genotypes. Each child would inherit one A allele from the AO parent and one B allele from the BO parent, resulting in the possible combinations of AO, BO, AB, or OO genotypes.
There is no way to be absolutely positive that your child will not have Morquio's syndrome if both parents have the gene, but there are genetic screenings to help prevent having a child with Morquio's syndrome.
O- would be the only possible blood type for the child.
Having a sibling with Down syndrome does not directly increase the chances of giving birth to a child with Down syndrome. The risk is influenced by maternal age, not family history. If both parents are carriers of the genetic translocation for Down syndrome, the risk may be higher.
Yes! The genotypes of the parents can only be "OO" (means two O genes) so both of them cannot give a "B" gene to the child
Yes, it is quite possible. It does require both parents to have AO(+-) genotypes, which is somewhat rare, however.
Since Down Syndrome is not genetic and is a trisomy, dominant and recessive genes do not play a role and it is possible for two down syndrome parents to have a child without down syndrome.
Yes. It would take too long to explain genotypes and phenotypes, just know that it is possible.
No, it is possible for 2 parents with down syndrome to produce a child with no non-disjunction disorder because of a gamete is produced with an extra copy of the chromosomes.
Yes, it is possible. Parents who are O positive may have children who are O+ or O-, depending on the parents' genotypes.
No. Parents who have a child with Down syndrome do not have an increased chance in having another child with Down syndrome. Everyone has the same chance of having a child with Down syndrome, 1%.
Yes, it's possible but there are very slim chances. It depends heavily on the genotypes of both parents
Yes, it's possible but there are very slim chances. It depends heavily on the genotypes of both parents
A child can develop Marfan syndrome even if their parents are not carriers due to a new mutation in the FBN1 gene, which is responsible for the condition. This spontaneous mutation can occur during the formation of the egg or sperm or shortly after fertilization, leading to the child exhibiting symptoms of Marfan syndrome despite having no family history of the disorder. Additionally, Marfan syndrome has a variable expressivity, meaning that not all carriers may show symptoms, making it possible for parents to be unaffected while still having a child with the condition.
If the parents had the genotypes AO and BO, then they could have a child with Type O blood (there would be a 25% chance of this occurring).
The children could have AO, BO, AB, or OO genotypes. Each child would inherit one A allele from the AO parent and one B allele from the BO parent, resulting in the possible combinations of AO, BO, AB, or OO genotypes.
There is no way to be absolutely positive that your child will not have Morquio's syndrome if both parents have the gene, but there are genetic screenings to help prevent having a child with Morquio's syndrome.