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.
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.

Related Questions

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

SICKLE CELL AFFECTS . With sickle cell the spleen can be destroyed by the crisis episodes. Read more...
See below. Sickle cell produces an abnormal hemoglobin that sickles in various circumstances (like fever or cold weather). Bea-thalassemia produces decreased amounts of hemoglobin, causing an abnormal arrangement of hemoglobin within the red cell. Both can have variable disease severity. 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...

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. Read more...

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...

Do hb e/beta thalassemia anemia reduce life expectancy?

Not necessarily. Did you look at the website reference i sent? It is quite informative. You will be best served with a visit to a specialist to get all your questions answered. It is clear you are so worried about this, and it would be so much more reassuring to have a face to face visit with someone who can answer all your great questions. 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...