Anemia can affect individuals of all ethnicities, but certain types are more prevalent in specific populations. For example, sickle cell anemia is more common among people of African and Mediterranean descent, while thalassemia is often found in individuals from Mediterranean, Middle Eastern, and Southeast Asian backgrounds. Iron deficiency anemia can occur across all ethnicities but may be more prevalent in populations with limited access to iron-rich foods or healthcare. Overall, genetic, environmental, and dietary factors contribute to the variations in anemia prevalence among different ethnic groups.
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Caucasian
Sickele-Cell Anemia ia one one of the most common genetic blood disorders.
Aside from joint problems, anemia is one of the more common problems in people with RA. As many as 60% of R A sufferers are anemic.
Sickele-Cell Anemia ia one one of the most common genetic blood disorders.
sickle cell anemia
Angelman syndrome does not appear to be more common in any specific ethnicity; it affects individuals across all ethnic backgrounds equally. The condition is caused primarily by genetic mutations, particularly deletions or mutations in the UBE3A gene on chromosome 15, which occur randomly. While there may be variations in reporting and diagnosis rates among populations, there is no significant evidence to suggest that one ethnicity is more predisposed to Angelman syndrome than others.
While technically there are more than one, the main one by far is sickle cell anemia.
There are several types of anemia. The term means without blood. It could be caused by excessive bleeding or damage to the bone marrow. Anemia is one of the most common disorders of the blood. It can be due to excessive blood loss or hemorrhage. Or deficient red blood cell production. Anemia can be classified in several ways: macrocytic anemia, normocytic anemia, microcytic anemia. Some of the more familiar ones are: pernicious anemia due to lack or low B12, iron deficiency anemia due to lack of iron, thalassemia, lead toxicity anemia, hypothyroidism, aplastic anemia, sickle cell anemia, Rh disease, and renal infection among others.
The original term for cooley's anemia, is Mediterranean anemia. People from the Mediterranean origin tend to develop this disease more commonly. Children can inherit it from one of their parents.
yes
One gene controlled one trait within Mendel's study, but the sickle cell anemia effects more than one trait.