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Sickle cell generally affects those of African origin, more specifically those whose parents are from areas where malaria is common

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10y ago

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What Sickle cell disease is and which population?

sickle cell occurs in populations more toward africa, just like malaria.


Is sickle cell disease a blood cancer?

No, sickle cell disease is not cancerous.


Is you kiss do you get sickle cell disease?

No. Sickle Cell is not an infectious disease, but is genetic.


What is the probability of am man and woman giving birth to a child who to is sickle cell like both of them?

If both parents are carriers of the sickle cell trait (genotype AS), there is a 25% chance that their child will inherit the sickle cell disease (genotype SS). Each parent has one normal hemoglobin allele (A) and one sickle cell allele (S), which means the possible combinations for their child are AA, AS, and SS. Therefore, the probability of the child being affected by sickle cell disease is 25%. If both parents have sickle cell disease (genotype SS), then all children will also be affected (100%).


What are other names for sickle cell anemia?

Hemoglobin SS disease (Hb SS)


How prevalent is the disease sickle cell in the population?

its a very rare disease because you have to be heterozygous to have it! I KNOW I'M CLEVER


What genetic disorder results in abnormally shaped blood?

Spherocytosis


How can sickle-cell disease be treated?

Stem cell or bone marrow transplants are the only cure for sickle cell disease


Why do African Americans get affected by sickle cell anemia?

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.


Top 10 questions asked about sickle cell?

What is sickle cell disease?Sickle cell disease is an inherited disorder that affects red blood cells. People with sickle cell disease have red blood cells that become hard and pointed instead of soft and round. Sickle cells cause anemia, pain and many other problems.Top2) What is sickle cell trait?If you have sickle cell trait, you have inherited the gene for sickle cell disease. Sickle cell trait does not turn into sickle cell disease. If someone has sickle cell trait and his partner has sickle cell trait they may produce a child with sickle cell disease. There are about 2.5 million people in America with sickle cell trait.Top3) If sickle cell trait is not an illness, why are people tested?Babies are tested to see if they have sickle cell disease. Teens and adults are tested mainly to see if they can have a baby with the disease.Top4) What medical problems are caused by sickle cell disease?Lung tissue damage, pain episodes and stroke. The blockage of blood flow caused by sickled cells also causes damage to most organs including the spleen, kidneys and liver.Top5) How many people have sickle cell disease?Sickle cell disease is a global health problem. In the United States it is estimated that over 70,000 people have sickle cell disease. About 1,000 babies are born with the disease each year in America.Top6) How long does a person with sickle cell disease live?The average life expectancy in America has improved. It is now in the mid 40 years of age range.Top7) Are people of African descent the only group affected?No. It is also present in Portuguese, Spanish, French Corsicans, Sardinians, Sicilians, mainland Italians, Greeks, Turks and Cypriots. Sickle cell disease also appears in Middle Eastern countries and Asia.Top8) Is there a cure?There is no universal cure for sickle cell disease. Research in gene therapy, the ultimate universal cure, is currently underway.Top9) What are some promising treatment developments?The use of hydroxyurea has shown promising results on some adult sickle cell patients. It reduces the frequency of severe pain, acute chest syndrome and the need for blood transfusions.Top10) Can people with sickle cell disease live a productive life?Yes. But like all patients with chronic disease, sickle cell patients are best managed in a comprehensive multi-disciplinary program of care and a strong extended support system.


What are the different types of sickle cell disease and how do they differ from each other?

There are several types of sickle cell disease, including sickle cell anemia, sickle beta thalassemia, and sickle cell-hemoglobin C disease. These types differ based on the specific genetic mutations that affect the hemoglobin protein in red blood cells. Sickle cell anemia is the most common and severe form, where individuals have two copies of the sickle cell gene. Sickle beta thalassemia and sickle cell-hemoglobin C disease are milder forms that result from different combinations of genetic mutations. Symptoms and complications can vary among the different types of sickle cell disease.


How do doctors diagnose sickle cell disease?

bone marrow transplant is the only known cure of sickle cell disease.