Sickle Cell Life Expectancy at Life

Sickle Cell Life Expectancy. Approximately 100,000 americans are living with sickle cell disease and have a lower mean life expectancy of 40 years. Sickle cell disease (scd) is a common genetic disorder with potentially devastating consequences for those afflicted.

It is a long way to parity for those born with sickle cell disease. The average life expectancy in the developed world is 40 to 60 years. Sickle cell disease is an inherited red blood cell disorder that affects about 100,000 americans, mostly of african or hispanic descent.

Sickle Cell Anemia. Student Presentation

Overall, the life expectancy for someone with sickle cell disease tends to be shorter than normal, but this can vary depending on the exact type of sickle cell disease they have, how it's treated and what problems they experience. In one study, the median survival time in patients with scd after the diagnosis of esrd was about 4 years, and the median age of death after diagnosis was 27 years, despite dialysis treatment. Bone marrow transplantation is the only treatment option for the sickle cell anemia, but this is a difficult and risk method. In america, life expectancy in cases of women with sickle cell anemia is 48, while men are expected to live until he turns 42 years.