Ad
related to: sickle cell life expectancy- Learn About Treatment
Learn About the Treatment Journey.
Watch the Video to Learn More.
- Patient FAQs
Get Answers to Common Questions.
Understand the Potential Risks.
- Safety and Side Effects
Review the Important Safety
Information & Side Effects.
- View Discussion Guides
Download Treatment Brochures,
Discussion Guides, and More.
- Patient Information
View Important Patient Information.
Understand the Treatment.
- Find an ATC
Find an Authorized Treatment Center
On the Official Patient Website.
- Learn About Treatment
Search results
Results From The WOW.Com Content Network
Autosplenectomy can occur in cases of sickle-cell disease where the misshapen cells block blood flow to the spleen, causing scarring and eventual atrophy of the organ. [2] Autosplenectomy is a rare condition that is linked to certain diseases but is not a common occurrence. It is also seen in systemic lupus erythematosus (SLE).
While 65-year-old black men had a lower total life expectancy (11.4 years) and active life expectancy (10 years) than white men (total life expectancy, 12.6 years; active life expectancy, 11.2 years), those differences were reduced when controlling for education.
The total life expectancy for males and females at birth was estimated at 62 and 66 years, respectively, and this is considered the average for least developed countries. The under-five child mortality rate was 77/1000 in 2015 compared to 128/1000 in 1990 and the maternal mortality ratio was 360/100,000 in 2015 compared to 720/100,000 in 1990.
This would be similar to the hemoglobin allele which is responsible for sickle-cell disease, but solely in people with two copies; those with just one copy of the allele have a sickle cell trait and gain partial immunity to malaria as a result. This effect is called heterozygote advantage. [27]
Diamond–Blackfan anemia (DBA) is a congenital erythroid aplasia that usually presents in infancy. [3] DBA causes low red blood cell counts (), without substantially affecting the other blood components (the platelets and the white blood cells), which are usually normal.
Congenital hemolytic anemia (CHA) is a diverse group of rare hereditary conditions marked by decreased life expectancy and premature removal of erythrocytes from blood flow. Defects in erythrocyte membrane proteins and red cell enzyme metabolism, as well as changes at the level of erythrocyte precursors, lead to impaired bone marrow erythropoiesis.
Ad
related to: sickle cell life expectancy