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What else can I help you with?
Is it possible in rare cases to have A plus group of child if both parents are O plus?
The only way that would be possible is if there was a mutation during the formation of one or both of the parents' gametes.
When a child is born with a chromosomal mutation when did mutation occur?
during meiosis
When a child is born chromosomal mutation when did the mutation occur?
During meiosis
When a child is born with a chromosomal mutation when did the mutation occurs?
during meiosis
Can two people with dimples have a child with dimples?
There is a 50% chance of a child having dimples if one parent has them and a 75% chance if the two parents have them. A child can also have them as the result of a genetic mutation even if neither parent has dimples.
Can PID be transmitted to a child during pregnancy?
PID can't be transmitted to a child during pregnancy.
How is albinism inherited and passed down through generations?
Albinism is a genetic condition that is inherited when both parents carry a specific gene mutation. This mutation is passed down through generations in an autosomal recessive pattern, meaning that both parents must pass on the mutated gene for a child to have albinism.
How can a child whose parents are not carriers get Marfan syndrome?
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.
How would a child inherit PKU?
A child inherits PKU if both parents are carriers of the gene mutation that causes the condition. When both parents are carriers, there is a 25% chance with each pregnancy that the child will inherit two copies of the mutated gene and have PKU.
Can a person pass their mutation to their child?
possible but unlikely
How is cockayne syndrome passed down from parent to offspring?
CS is inherited in an autosomal recessive pattern. In order for a child to be affected by CS, he or she must inherit a mutation (-) in the same CS gene from both parents. The parents and other "carriers" of a single CS gene mutation remain healthy. Once a couple are known to carriers, they have a 1 in 4 (25%) chance of having another child with CS. http://www.cockaynesyndrome.net/main/AboutCS.aspx
If child is born with trisomy when did the mutation occur?
during meiosis
