What's the life expectancy of someone with sickle cell anemia?

Shortened. . Depends on the complications experienced as a child. Those with numerous complications will love shorter lives than those without complications. Those without complications can live into their 60s the average lifespan of someone with sickle cell is probably in the mid to late 40s we are still trying to understand why some people have so many troubles and others do not.

Related Questions

What would the life expectancy of someone with sickle cell anemia be?

Shorter than average. It depends on the type and severity of the sickle cell anemia that you have and all complications related to the sickle cell anemia- i.e.Acute chest syndrome, strokes, avn, mi, etc. The life expectancy is unfortunately shorter than average population- in hb ss sickle cell anemia- on average it's around 40- 50 yrs of age. The more severe and more complications - the shorter the life span would be. Read more...

What is the life expectancy with sickle cell anemia?

40-50 years. One survey i found stated that the median life expectancy for people with sickle cell disease is 42 years for men and 48 years for women. Keep in mind that those numbers represent the age at which half of the people die - so many people can live much lomger with good medical care and taking very good care of themselves. Read more...
close to normal . Scd is many types , the most severe is the ss-disease . Even among patients with ss disease, there are risin the past it was about 4decades. With the improved care, prevention of serious complications by early diagnosis, blood transfusion, exchange for stroke patients and the use of hydroxy urea, life expectancy is becoming close to normal in many patients with scd who are under good medical care. Read more...

Do beta thalassemia and sickle cell anemia always reduce life expectancy?

Not if just 1 trait. Having either beta thalassemia trait or sickle cell trait is a mild condition and should not cause symptoms to the point of making a person frequently ill nor shortening life expectancy. Having beta thalassemia major or sickle cell disease, or both sickle cell trait and beta thalassemia trait, usually causes severe enough chronic disease symptoms to shorten lifespan an uncertain amount. Read more...
Life expectancy . With clinically significant sickle syndromes or thalassemia syndromes is lower than for people without these afflictions, but are improving all the time. If you have trait for either condition, it should not have a measurable impact on your life expectancy. Read more...

What's the life span of someone with sickle cell anemia?

Variable . The problem with sickle cell anemia is prognosis varies. Most are living longer because of better infection control, newer medication like hydrea, (hydroxyurea) and improved follow up managment. Some patients can have sickle cell and greater levels of hbf and they tend to do better. Predictors can include sausage digits, stroke, renal failure, anemia level less then 7, leukocytosis. The best answer is it varies. Read more...

If you are a carrier of sickle cells does it affect you like someone with sickle cell anemia?

Generally no. A "carrier" inherited the sickle trait from one parent. Sickle cell anemia (ssa), occurs in those who inherit the sickle cell gene from both parents. This is associated with a variety of serious symptoms. The problem with trait is that if your partner also has it you can pass on ssa to a child. Rarely being a carrier causes symptoms but generally much more mild than with ssa. Read more...
Altitude. Generally no. There are many cases of spleen problems noted in sickle cell carriers when they come to high altitude. This typically causes abdominal pain and a sudden loss of red blood cells (they get trapped in the spleen). Typically this can occur with dehydration at altitudes of 8000 feet or more. Read more...
No. The presents of a normal gene next to the sickle gene allows the DNA to manage creation of hemoglobin that functions normally under most circumstances. Read more...

How does gene therapy be used to cure someone with sickle cell anemia?

Replace gene. Gene therapy could be used to transfer a new replacement normal gene to cells producing red blood cells. That is how gene therapy would work however there are no approved gene therapy treatments for sickle cell anemia. Read more...