have seen one of my friends sister had kid and all normal no complications...not thalassemia either.........beta and alpha i think there is 25% normal chance
If only the mother has the thalassemia trait, each child has a 50% chance of inheriting the trait and becoming a carrier, and a 50% chance of being unaffected. The father’s genotype will determine the overall risk for the children. If the father does not have thalassemia or the trait, the children will only be carriers. However, if the father also carries the trait, there is a possibility of having children with thalassemia disease.
It is unlikely.
If you have beta thalassemia trait and your partner has sickle cell trait there is a 25% chance of your child having sickle beta thalassemia.
Thalassemia is classified mainly into two types: alpha thalassemia and beta thalassemia, based on which globin chain is affected. Alpha thalassemia occurs due to mutations in the alpha-globin genes, while beta thalassemia results from mutations in the beta-globin genes. Each type can further be categorized into various subtypes based on the severity of the condition, such as thalassemia minor (trait) and thalassemia major (Cooley's anemia). The classification helps determine the appropriate management and treatment strategies for affected individuals.
you have a 50/50 chance me and my twin both had it and my 2 older brothers are fine 1 is a carrier and the other is not.
Thalassemia trait, also known as alpha or beta thalassemia minor, is a genetic condition characterized by a reduced production of hemoglobin. Individuals with this trait typically have normal or slightly reduced hemoglobin levels, and they do not usually suffer from iron deficiency. Therefore, taking iron supplements can lead to iron overload, potentially causing damage to organs, as the body does not require additional iron in this condition. It's essential for individuals with thalassemia trait to consult healthcare professionals before taking iron supplements.
Yes, Thalassemia sex is a linked trait. Ha ;)
Very unlikely. Thalassemia is an inherited disease, affected persons are born with the genetic disorders. However, silent carriers (Alpha Thalassemia, 1 gene defect) or Beta Thalassemia Trait (1 gene defect), do not have significiant symptoms. Consequently, if this person did not have any relevant blood tests till the age of 20, he/she might no be aware of having the condition. That's only a hypothetical suggestion.
Yes.... because blood trait A is dominant on blood trait O... the child will then have blood group A
father for sure, maybe the mother too
Thalassemia Intermedia is a recessive trait inherited disease of the red blood cells. In thalassemia, the genetic defect results in reduced rate of synthesis of normal hemoglobin chains.
Thalassemia trait, typically a genetic condition characterized by reduced hemoglobin production, usually doesn't worsen with age because it is a stable genetic trait. Individuals with thalassemia trait often maintain sufficient hemoglobin levels for normal function and experience few, if any, symptoms throughout their lives. While some may develop mild anemia, this does not typically progress to more severe forms or complications as they age. Regular check-ups can help manage any potential issues, but the trait itself remains stable.