Yes
Sickle cell anemia can't be prevented through medicine because it is a genetic trait. The only way to totally prevent it is to make sure that neither parent carries the trait.
77%
No, sickle cell anemia and sickle cell trait are not the same. Sickle cell anemia is a severe form of the disease caused by inheriting two sickle cell genes (one from each parent), leading to significant health complications. In contrast, sickle cell trait occurs when an individual inherits only one sickle cell gene and one normal gene, typically resulting in no symptoms but allowing the person to pass the trait to their offspring.
You are born with this trait. If you had both copies, instead of one, you would have the disease. There is no way to get rid of it. Think about any children you have and be sure the person who will be the other parent doesn't carry the trait or have the disease.
If one parent has sickle cell trait and the other parent has the normal type of hemoglobin, there is a 50% (1 in 2) chance with EACH pregnancy that the baby will be born with sickle cell trait.
because that persons grandma or grandpa or one of their past realatives could have had that trait
The sickle cell trait is that you dont have the whole thing you have half of it which is called the trait
once youdidn't get it from birth, then it is not possible to get it when you grown up, but if you want to protect your future children not get the disease than it is better not to married from sickle cell disease man
A child has to receive the gene from both parents to heve sickle cell anemia. if only one parent passes on the gene, then the child will have sickle cell trait, but no symptoms of sickle cell anemia.
The simplest form of genetic inheritance for a single trait involves receiving one
Recessively, that means that both parents must be symptomless carriers then there is only a 1 in 4 chance that a given child will be born with the disease. Note: symptomless carriers have the strong advantage of being much more likely to survive malaria than "normals". Sickle cell disease is inherited through a single pair of genes (one gene from each parent), on chromosome 11. They must receive the gene from both parents in order to actually get sickle cell disease. If they receive one gene for sickle cell disease from one parent but a normal gene from another, they have "sickle cell trait." The genes that involve sickle cell control the production of hemoglobin (a protein) in red blood cells. Abnormal hemoglobin from sickle cell disease causes red blood cells to grow incorrectly. Persons with sickle cell trait are much more resistant to malaria (a common disease in Africa, where the gene originated) than persons having two normal genes. This makes the sickle cell gene very likely to persist in areas where malaria is endemic, like Africa.
The person is homozygous for the trait