What are the different types of sickle cell anemia?

Types os SIckle Cell. From nih, division of blood diseases and resources: sickle cell disease-ss: 65% of us patients; genotype s/s sickle cell disease-sc: 25% of us patients; genotype s/c sickle cell disease-s beta + thalassemia: 8% of us patients; genotype betas/ beta + thalassemia sickle cell disease-s beta 0 thalassemia: 2% of us patients; genotype betas/ beta 0 thalassemia.
Two. Sickle cell anemia occurs when 2 abnormal hemoglobin genes are present and a person's body produces sickle cell hemoglobin exclusively. 1 sickle cell gene and a normal gene produce sickle trait, which has no symptoms. Other abnormal hemoglobin genes can combine with a sickle cell gene and produce other types of anemia. There are several other genetic hemoglobin abnormalities.

Related Questions

What are the types of gene defects in sickle cell anemia?

Several. There are several genetic defects that lead to sickle cell anemia. They all lead to a change in the 6th Amino Acid in the beta-globin chain in which valine is substituted for glutamic acid. At least 5 different dna mutations have been identified that all lead to the same Amino Acid substitution, and thus, sickle cell anemia. Read more...

What blood type is administered to those that have sickle cell anemia?

Type-specific. Type specific blood is given. In those patients who require blood transfusions very frequently, the providers often will expand the blood typing to include a number of addition blood typing systems. We call this an expanded phenotyping of blood. Read more...
Transfusions for SS. Blood transfusions are sometimes an essential part of treatment and prevention in sickle cell (ss) disease. The rules regarding what blood type to give are the same for those not affected by ss, however, it is very important to use a blood bank well-versed with ss patients. Ss patients can generate antibodies to rare red blood cell proteins, matching of which is essential for long-term management. Read more...

What type of genetic disorder is sickle cell anemia or trait?

Hemoglobinopathy. Patients with sickle cell anemia make an abnormal hemoglobin (hgb.). Normal HGB consists of paired protein chains (globin) and an iron containing part (heme). Patients with ssa inherit an abnormal beta-globin gene from each parent. Carriers have one normal beta-globin gene and one sickle beta globin gene. The carriers (trait) have no symptoms. Read more...

Should I consider my blood type when trying to conceive when sickle cell anemia runs in my family?

Cons your hemoglobin. You should consider whether or not you and the person you are conceiving with have sickle cell trait and/or other abnormal hemoglobin in order to estimate the risk to your offspring. Read more...
If you've never been. tested for sickle-cell trait, other hemoglobinopathy, G-6-PD Deficiency, MTHFR mutation or other inheritable disorder that runs in your family, do so now. If you test positive for an autosomal recessive disorder, your husband will also need to be tested.Start at least 4 micrograms of Folic Acid daily 3 months before conception & get a flu vaccine at least 2 months before conception. Read more...

What are the chances of a man with sickle cell anemia catching herpes simplex type 2 from someone that is not having an outbreak?

The same as others. You will have the same likelihood as someone who does not have sickle cell anemia (low, but not zero). Read more...
Not zero. Sickle cell anemia plays no role in this situation. The key point is that some individuals that have been infected with herpes simplex virus can have asymptomatic shedding of virus, even when not having an outbreak. Read more...

I have sickle cell anemia and wanted to know how to go about getting stem cell transplant, is there some type of waiting and who do I go through?

See BMT doctor. In someone your age, whether you can be transplanted or not would depend on many factors, the most important of which would be how well your organs are functioning (like liver, kidneys, heart). You also need a adequate donor. You have to see a bone marrow transplant doctor. Since you live in Georgia, I would recommend going to Emory to see an Adult or Pediatric Bone Marrow Transplant Doctor. . Read more...
Need a donor . Stem cell transplant is not a simple procedure and can carry significant risk. However it will cure sickle cell anemia. The biggest hurdle to transplant is finding a donor who matches you. You would have to be seen at a transplant center first to do the testing to see if a potential donor exists and to get insurance authorization. The center would also have to have a protocol for sickle cell. . Read more...