Anemia

Anemia, characterized by a deficiency in red blood cells or hemoglobin, can lead to reduced oxygen delivery to tissues. In response, the body compensates by increasing heart rate to maintain adequate oxygen levels and ensure proper blood circulation. This elevated heart rate is often referred to as compensatory tachycardia and can indicate the severity of anemia. Therefore, monitoring heart rate can help assess the impact of anemia on cardiovascular health.

The billing code for anemia varies depending on the specific type of anemia being diagnosed. Generally, the ICD-10 code for unspecified anemia is D64.9. However, for specific types such as iron deficiency anemia, the code would be D50.9. It's essential to use the correct code based on the diagnosis to ensure accurate billing and reimbursement.

Sickle cell trait itself typically does not qualify a child for Supplemental Security Income (SSI) benefits, as it is generally considered a genetic condition that does not significantly impair functioning or result in severe health issues. SSI is designed for individuals with disabilities that severely limit their ability to work or perform daily activities. However, if a child with sickle cell trait experiences severe complications related to the condition, they may be eligible for SSI based on those specific health challenges. It's important to consult with a qualified professional for a thorough evaluation of the child's situation.

Anemia can lead to a paler skin tone due to reduced hemoglobin levels and decreased oxygen delivery to tissues. This pallor is often most noticeable in areas with thinner skin, such as the face, palms, and nail beds. In some cases, individuals may also exhibit a yellowish tint, particularly if the anemia is related to liver issues or hemolysis. Overall, the skin may appear less vibrant and healthy.

Yes, A "carrier" of alpha thalassemia and of beta thalassemia can marry, but not to someone with any hemoglobinopathy.

Prof. Kornfeld Pal

Most definitely. The veterinary research shows about 50/50 chance. Survival odds are better if the dog survives the first few days.

Sickle-cell disease, usually presenting in childhood, occurs more commonly in people (or their descendants) from parts of tropical and sub-tropical regions where malaria is or was common. The prevalence of the disease in the United States is approximately 1 in 5,000, mostly affecting Americans of Sub-Saharan African descent. In simplified terms usually black people.

it's caused by a mutation in the hemoglobin gene(a weird change that's basically in the red blood cell)disease is a group of genetic dis orders caused by sickle hemolobin(hgb s or hb s(

Sickle-cell is inherited from parents just as physical traits. People with the disease are SS type and show the anemia. Others can carry the trait (Ss). They are able to fight off malaria. Since this type (Ss) is important in areas with many malaria cases, this is protective.

Yes, you don't bleed a lot when you get a piercing.

It is important to note that sickle-cell anemia comes in two forms. The homozygous sickle-cell anemia and the heterozygous sickle-cell trait. The difference between the two is that sickle-cell anemia has a high rate death rate at a young age (20~), and the sickle-cell trait is nearly asymptomatic.

In regions such as North America, sickle-cell anemia would be selected against and would eventually leave the gene pool. The sickle-cell trait on the other hand, has little effect on the fitness of the organism, and as such will remain in the gene pool.

In malaria endemic regions such as sub-Sahara Africa, sickle-cell anemia provides very high levels of immunity to malaria and the sickle-cell trait provides a slightly lesser level of immunity. Both forms of sickle-cell will increase the organisms fitness and as such, it will remain in the gene pool. Further on, the sickle-cell trait has greater fitness than sickle-cell anemia, hence, the sickle-cell trait will be selected as the fittest allele.


If s is the sickle-cell allele and S is a normal allele;

The relative fitness in malaria endemic regions;
Ss > ss > SS
Sickle-cell trait > Sickle-cell anemia > Normal

The relative fitness in non-malaria endemic regions;
SS > Ss > ss
Normal > Sickle-cell trait > Sickle-cell anemia

atropic gastritis

it is used in making tables chairs and many other handy things

like wiring and piping (not like icing )

Write a summary of the main ideas you covered in the essay.

the sickle trait possess a resistance to the infection of malaria.

Pernicious Anemia has to do with your red blood cells lacking a strong count because of a great vitamin B12 deficiency, either some through some illness, infection or other cause that makes your stomach to be unable to absorb the necessary about of B12 from your food. So the part of the body this has to do with is your circulatory system, which in turn affects everything.

A CBC, or complete blood count, is a clinical procedure that can aid in the diagnosis of leukemia and anemia. The peripheral blood smear can also be helpful in diagnosis.

The defect is that hemoglobin (the protein) elongates. Instead of being circular, it acquires a crescent shape. With this shape, its harder for it to absorb and release oxygen. Also, when the blood cell reaches the capillaries, it can't fit through as well as normal blood cells can, which is why Sickle-Cell is painful.

If you have Thalassemia major but your boyfriend is not a carrier then the child will be born a healthy carrier (thalassemia minor) but shouldn't need blood transfusions. If your boyfriend is a carrier then you would have a 50% chance of having a child with thalassemia major like you do.

prevaalence of anemia in India in the year 2010

No. Cancer by definition entails growth. A.A. is a destruction of the stem cells that produce blood. (Both may require the same treatment of a bone marrow transplant)