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Sickle cell anemia is a gentic disease carried by people of African and sometimes Indian decent. Although both parents need to at least carry the gene for their children to get it not necessarily have the disease.
It is 100% possible that a person who has two parents with the disease will be a carrier of the defective gene.
Someone can catch hemolytic anemia from their parents. When a child is born and if the parents possess this condition, it can be passed on to the child.
Sickle cell anemia was discovered in the 1870's and carried many names, but 1922 it was officially named sickle cell anemia.
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The original term for cooley's anemia, is Mediterranean anemia. People from the Mediterranean origin tend to develop this disease more commonly. Children can inherit it from one of their parents.
In general it is called anemia but the causes varies from case to case
Sickle cell anemia is a inherited blood disorder. This means everyone who has sickle cell has inherited it from their parents. With this in mind it means there was a key ancestor in Africa or the Mediterranean who had the first sickle cell anemia and passed it on to their descendants.
Sickle Cell Anemia would be a genetic ailment because it is passed down from the parents.
The parents are both recessive (Ss) for sickle cell anemia.
The parents are both recessive (Ss) for sickle cell anemia.
A normal homozygous individual can't produce offspring with sickle cell anemia. Both parents must carry the trait to have an offspring with the illness.