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What else can I help you with?
How can you decrease chances of getting sickle cell anemia?
Sickle cell anemia is a genetic disease. There is nothing you can do after you're born to reduce the risk.
Are there prenatal tests for sickle cell anemia?
Yes, there are prenatal tests for sickle cell anemia, which can be performed during pregnancy to determine if the fetus has the condition or carries the sickle cell trait. Common methods include chorionic villus sampling (CVS) and amniocentesis, both of which analyze fetal DNA. Additionally, non-invasive prenatal testing (NIPT) can assess the risk of sickle cell disease based on the parents' genetic profiles. These tests help parents make informed decisions regarding their pregnancy and potential management options.
What is the advantage of being heterozygous for the sickle cell allele?
Sickle cell trait carries a lower risk of serious malarial disease, without the signs and symptoms of sickle-cell anemia.
How does a person with one sickle cell different than two Sickle cell?
A person with one sickle cell is a "carrier". This means that they have the dormant cell in their genetic composition, and if combined with another with the "carrier" gene, they run the high risk on concieving a child with the blood disease-one who has two sickle cells. A person with two sickle cells, has the sickle cell disease and are carriers(The gene is not dormant but active). Hope this simplifies and explains it for you.
If you have sickle cell and get treated for chlamydia what would happen?
You would lower your risk of complication from untreated chlamydia.
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.
Why D5W in a sickle cell patient?
D5W (5% dextrose in water) is often used in sickle cell patients to prevent dehydration and maintain adequate hydration levels. Sickle cell disease can lead to increased red blood cell destruction, which can result in dehydration and an increased risk of sickling episodes. D5W provides a source of glucose for energy and helps prevent the sickling of red blood cells by maintaining proper fluid balance in the body. Additionally, D5W is isotonic, meaning it has a similar osmolarity to blood, reducing the risk of hemolysis and other complications in sickle cell patients.
What are the benefits of sickle cell trait?
sickle cell trait is caused by two recessive alleles - meaning both partns must give resessive trait DNA o their child. - sickle cell anemia dose not have a benefit - or if it dose it is out waysd by the fact that people with sickle cell have very low blood oxygen as their blood cellsare dis-formed. however, if there is only one allele- ie they have A and b alleles for sickle cell. then they are more immune to malaria. a deadly parasite passed by misquotes in tropical countries.
Does the environment play a role in sickle cell anemia?
Yes, the environment can play a role in sickle cell anemia by affecting factors such as hydration, temperature, and altitude that can trigger sickling of red blood cells and potentially lead to complications. Staying well-hydrated, avoiding extreme temperatures, and adjusting to high altitudes can help manage symptoms and reduce the risk of sickle cell crises in affected individuals.
Are the offspring of parents who are both homozygous dominant for normal red blood cells in danger of getting sickle-cell anamia and why?
No, if both parents are homozygous dominant for normal red blood cells, their offspring will inherit two normal alleles and will not be at risk of developing sickle cell anemia. Sickle cell anemia is a recessive genetic disorder that occurs when an individual inherits two copies of the mutated allele.
Can mixed race get sickle cell disease?
lol that's a dumb question and that's a dumb answer. Yes it is always possible, to some tiny degree. The risk factor is dependent on the specific races involved. For example a person of African decent has a higher risk, than a person of hispanic or Mediterranean, and caucasian is the lowest risk of all. If one parent is caucasian the risk is pretty small. among 2 caucasians, not of middle eastern or Mediterranean, non jewish, the risk is smallest.
The mutation that results in sickle cell anemia produces effects that are?
The mutation that causes sickle cell anemia leads to the production of abnormal hemoglobin, which causes red blood cells to become sickle-shaped. These sickle-shaped cells can block blood vessels, impairing blood flow and leading to episodes of pain, tissue damage, and increased risk of infections.
