Can white people get sickle cell?

Sickle cell disease affects millions of people around the world. While it's very common in people of African heritage, people of other races and ethnicity can also inherit the condition. For example, white people can get sickle cell disease.
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Do only black people get sickle cell?

Answer. Yes, they can. Sickle cell disease can affect people of ANY race or ethnicity. Sickle cell disease, an inherited disorder of the red blood cells, is more common in African Americans in the U.S. compared to other ethnicities—occurring in approximately 1 in 365 African Americans.
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What races can get sickle cell?

Sickle cell disease is more common in certain ethnic groups, including:
  • People of African descent, including African-Americans (among whom 1 in 12 carries a sickle cell gene)
  • Hispanic-Americans from Central and South America.
  • People of Middle Eastern, Asian, Indian, and Mediterranean descent.
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What percent of white people have sickle cell trait?

Among sickle cell trait births, 7.0% were white, 5.3% were multiracial, and 5.9% had unknown race. The relative distribution of race for each hemoglobin status remained relatively constant over time.
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Why is sickle cell more common in Africa?

The disease is most common in sub-Saharan Africa, where as many as 45% of people are carriers. It has become so widespread there because being a carrier offers a survival advantage against malaria. The Middle East doesn't really have a malaria problem, and the overall sickle-cell carrier rate is low.
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Midday Minutes: sickle cell disease affects Black people more than other racial groups



What country has the highest rate of sickle cell disease?

Nearly 90 percent of the world's SCD population lives in three countries: Nigeria, India, and the Democratic Republic of Congo (figure 1), where the disease affects up to 2 percent of the population, and the carrier prevalence rate (sickle cell trait) is as high as 10 to 30 percent [3,4,9,10].
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How long do sickle cell patients live?

Results: Among children and adults with sickle cell anemia (homozygous for sickle hemoglobin), the median age at death was 42 years for males and 48 years for females. Among those with sickle cell-hemoglobin C disease, the median age at death was 60 years for males and 68 years for females.
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Is sickle cell curable?

Stem cell or bone marrow transplants are the only cure for sickle cell disease, but they're not done very often because of the significant risks involved. Stem cells are special cells produced by bone marrow, a spongy tissue found in the centre of some bones. They can turn into different types of blood cells.
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What gender is most affected by sickle cell anemia?

No sex predilection exists, since sickle cell anemia is not an X-linked disease. Although no particular gender predilection has been shown in most series, analysis of the data from the US Renal Data System demonstrated marked male predominance of sickle cell nephropathy in affected patients.
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At what age does sickle cell manifest?

People with sickle cell disease (SCD) start to have signs of the disease during the first year of life, usually around 5 months of age.
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What is the difference between sickle cell anemia and sickle cell disease?

Sickle cell disease (SCD) is a serious group of conditions which are inherited (genetic). It affects the red blood cells in the blood. Sickle cell anaemia is the name of a specific form of SCD in which there are two sickle cell genes (see below).
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Why does sickle cell affect black?

So why are African Americans Affected More? SCD and SCT impact African Americans at disproportionate rates. This is simply because they both are evolutionary traits that individuals develop in response to help protect them from malaria. Around 50% of the global population live in areas where malaria exists.
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What kills sickle cell?

Sickle cell disease can cause organ damage, stroke and even death. When organs are deprived of oxygen, pain is just one consequence. Another is organ damage—to the liver, heart, kidneys, gallbladder and eyes—and even stroke.
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Can sickle cell be reversed?

There is no widely available cure for sickle cell disease. Some children with the disease have been successfully treated with blood stem cell, or bone marrow, transplants. This approach, though, was thought to be too toxic for use in adults.
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How old is the oldest person with sickle cell?

There are people with sickle cell living well past the average life expectancy. The oldest person currently living with sickle cell, Asiata Onikoyi-Laguda, is 94.
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Is sickle cell painful?

Periodic episodes of extreme pain, called pain crises, are a major symptom of sickle cell anemia. Pain develops when sickle-shaped red blood cells block blood flow through tiny blood vessels to your chest, abdomen and joints. The pain varies in intensity and can last for a few hours to a few days.
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What is the age limit for sickle cell?

Results. Among children and adults with sickle cell anemia (homozygous for sickle hemoglobin), the median age at death was 42 years for males and 48 years for females. Among those with sickle cell-hemoglobin C disease, the median age at death was 60 years for males and 68 years for females.
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Why sickle cell is common in Nigeria?

The prevalence of the sickle cell trait in many tropical African countries including Nigeria ranges between 20 and 30% of the population [9-12]. SCT is common in regions with high malaria endemicity as it confers a survival advantage against malaria [3, 4].
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How did sickle cell anemia start?

The origin of the mutation that led to the sickle-cell gene derives from at least four independent mutational events, three in Africa and a fourth in either Saudi Arabia or central India. These independent events occurred between 3,000 and 6,000 generations ago, approximately 70-150,000 years.
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Does sickle cell worse with age?

Because SCD is a genetic disease, people must be born with it. Children begin showing symptoms around 5 months old. Symptoms and complications then tend to get worse with age. The transition from pediatric to adult care is also linked to more medical problems.
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Can I marry a sickle cell woman?

And definitely, SS and SS must not marry since there's absolutely no chance of escaping having a child with the sickle cell disease. The only thing that can change the genotype is the bone marrow transplant (BMT).
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Does sickle cell anemia make you skinny?

Do you feel like you have control over your weight? Sickle cell patients typically have a slim physique and tend to struggle when it comes to gaining weight.
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Can babies have sickle cell?

Sickle cell anemia is caused when a baby gets one sickle cell gene change from each parent. Hemoglobin SC. This condition is caused when a baby gets one sickle cell gene change from one parent and one gene change for hemoglobin C (another abnormal type of hemoglobin) from the other parent.
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What percentage of sickle cell patients are black?

African Americans (8 to 10 percent of African Americans have sickle cell trait)
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Can you develop sickle cell anemia later in life?

“Individuals are born with the condition, which they inherit from both of their parents. A person cannot 'catch' sickle cell disease from someone who has it or develop the condition later in life if they do not have it at birth,” says Dr.
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