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Sickle-Cell Disease

Sickle-cell disease is a genetic blood disorder wherein the red blood cells are irregularly shaped due to the blood’s lowered oxygen tension. This irregularity may result in chronic anemia, serious infections, painful conditions, damage to organs and death.

538 Questions

Is sickle cell anemia an example of pleiotropy?

Pleiotropy describes the genetic effect of a single gene on multiple phenotypic traits. The underlying mechanism is that the gene codes for a product that is for example used by various cells, or has a signalling function on various targets. A classic example of pleiotropy is the human disease PKU (phenylketonuria). This disease can cause mental retardation and reduced hair and skin pigmentation, and can be caused by any of a large number of mutations in a single gene that codes for an enzyme (phenylalanine hydroxylase) that converts the amino acid phenylalanine to tyrosine, another amino acid. Depending on the mutation involved, this results in reduced or zero conversion of phenylalanine to tyrosine, and phenylalanine concentrations increase to toxic levels, causing damage at several locations in the body. PKU is totally benign if a diet free from phenylalanine is maintained.

Sickle cell anemia and some nerve and brain disorders are examples of which of these?

Sickle cell anemia and some nerve and brain disorders are examples of inherited diseases. These inherited diseases pass from parent to child via chromosomal exchange.

What does it mean when someone carries the sickle cell gene but does not have the disease?

If you carry the sickle cell gene, it doesn't really mean much as far as your own personal health goes. Except that you are less likely to get malaria. However, if you decide to have kids, and whoever you mate with also carries the sickle cell gene (not the full blown disease/gene) , your child has a chance of having sickle cell disease (full blown).

What type of mutations exist in sickle cell allele?

The sickle cell allele can have a point mutation where a single nucleotide is changed, resulting in the substitution of glutamic acid with valine in the beta-globin chain of hemoglobin. This leads to the characteristic sickle-shaped red blood cells in individuals with sickle cell disease.

Are people with Sickle cell disease immune to west nile virus?

People with sickle cell disease are not immune to West Nile virus. However, they may be at a higher risk for severe complications if they do contract the virus due to their weakened immune system. It is important for individuals with sickle cell disease to take precautions to prevent mosquito bites and reduce their risk of being infected with West Nile virus.

In the African tropics the maintenance of the sickle-cell allele in the human population can be attributed to?

Heterozygotes - those with sickle cell trait - show resistance to malaria. Therefore the survival rate of those with one sickle cell allele is higher than those with none - allowing for the trait to be passed on more frequently.

Sickle cell anemia results from a defective?

Sickle cell disease is a group of disorders that affects molecule in red blood cells (hemoglobin) that delivers oxygen to cells throughout the body. Person with this disorder have typical hemoglobin molecules called hemoglobin S, which can distort red blood cells into a sickle, or crescent, shape.

The HbS allele sickle cell occurs at a higher frequency in Africa than it does in the US because?

The higher frequency of the HbS allele in Africa is due to historical selective pressure from malaria. People with one copy of the HbS allele have increased resistance to malaria, providing a survival advantage in regions where the disease is prevalent. In the US, where malaria is not as common, there is less selective pressure for the allele to be maintained at high frequencies.

What is the major difference between thalassemia and sickle cell anemia?

Thalassemia is a quantitative problem of too few globins synthesized, whereas sickle-cell anemia (a hemoglobinopathy) is a qualitative problem of synthesis of an incorrectly functioning globin. (wikipedia)

Who is affected by sickle cell anemia?

Sickle cell anemia is a genetic blood disorder affecting individuals who inherit two copies of the abnormal hemoglobin gene from both parents. This primarily affects people of African, Mediterranean, Middle Eastern, and South Asian descent.

What is the causative agent of sickle cell?

Sickle cell disease is caused by a mutation in the gene that encodes for hemoglobin, a protein in red blood cells that carries oxygen. This mutation results in the production of abnormal hemoglobin known as hemoglobin S, which causes red blood cells to become sickle-shaped and less flexible.

Is sickle cell anemia dominant recessive x-linked recessive a chromosomal error or a multi-factorial trait?

Sickle cell anemia is a recessive genetic disorder caused by a mutation in the HBB gene, located on chromosome 11. It is inherited in an autosomal recessive pattern, meaning a person needs to inherit two abnormal copies of the gene (one from each parent) to have the disease. It is not an X-linked disorder or a multifactoial trait.

What is the definition of cell?

A cell is a little group of tissues that work together to create an organ which goes to the organ system to the organism.
A cell is a fundamental unit of life that is a small, membrane-enclosed unit that can grow, respond to it's environment, convert energy from one form to another, and reproduce. (cells are extremely diverse).
DEFINITION: A cell is the smallest and most basic structured component of an organism. Cells are in all organisms.

MORE DETAIL: There are many different types of cells that are found within organisms. This is because there needs to be certain cells that provide certain functions for different parts of the body.
A cell is the structural function and biological unit of any organism.
a cell is a part of an organisem that helps the body survive a cell is the basic unit af life

Condition of being heterozygous for a recessive trait?

If you are heterozygous this means you carry both a dominant and recessive allele. if you are heterozygous for a recessive trait then you will have a dominant and recessive allele. example: let T represent tall and t represent short. a person with heterozygous for a recessive trait will have 'Tt'.

How is it possible for only some races to have certain diseases or deformities like Sickle-Cell Anemia for African-Americans and Head Lice for Caucasians?

Some diseases are the result of adaptations to an environment. As it turns out, Sickle Cell Anemia is an adaptation to Malaria. If a person has a single copy of the Sicke Cell gene, he or she is protected against Malaria. If he or she has NO copies of the gene, he or she will die if exposed to Malaria. If he or she has two copies of the gene he or she will die from Sickle Cell Anemia. Malaria was fatal to pretty much everyone. The genetic mutation allowed about half of the population of the region to live. Today, we no longer have the threat from Malaria so now Sickle Cell Anemia becomes the problem.

How many people die of sickle cell?

Approximately 100,000 people die each year from complications of sickle cell disease, with most deaths occurring in sub-Saharan Africa. Early detection, proper management, and access to healthcare can help improve outcomes for individuals with sickle cell disease.

Is sickle cell anemia a point mutation?

An example of point-mutation is sickle-cell anemia. Sickle-cell disease is hereditary.

What do people affected with the sickle cell suffer with?

Peope with sickle cell disease suffer from pain crisis in arms,legs or ,chest. Well at least my daughter do. It is painful and she has to be admitted to hospital and receive morphine and. Iv fluids to relieve pain.

How can sickle cell be prevented?

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

If you mother and father are both sickle cell carriers what are the chances that you will not have the trait?

It is impossible to predict what will happen with one person!

In a population of 2,000 people, 1,000 women have sickle cell trait and 1,000 men do not. They marry. Each couple has 2 children. 1,000 children will have sickle cell trait and 1,000 children will not.

In a population of 2,000 people, 1,000 women have sickle cell trait and 1,000 men have sickle cell trait. They marry. Each couple has 2 children. 1,000 children will have sickle cell trait, 500 children will not, and 500 children will have sickle cell anemia.

No one knows which of those parents will produce which children. No one knows how to predict how your children will turn out.

Why cant people with sickle cell do a lot of exercise?

Exercising cost lot of energy.So Oxygen requirement increase.People with sickle cells, do not have normal number of blood cells to carry Oxygen.So energy production would not be sufficient.

What are the dangers of alcohol abuse and sickle cell trait?

People who have sickle cell should try to avoid consuming alcohol if at all possible. This is because sickle cell causes the patient to become dehydrated in the first place, so drinking alcohol would only exacerbate the problem.

Is sickle cell an dominant or recessive?

Sickle cell anemia is an autosomal recessive disorder. It can result from two carriers having a child together.