What is Srpk's hemoglobin?

Hemoglobin, also referred to as S. hemoglobin, is a common form of abnormal hemoglobin, which serves as a source for both anemia of sickle cells. Predominantly found in individuals of African origin, the presence of sickle hemoglobin, also called a sickle gene, can only be confirmed by a blood test. In cases where the inheritance of the sickle genes leads to anemia of sickle cells, there is no remedy for disease - there are only preventive measures to avert the pain crisis and the treatment of pain treatment, which may take hours or days, depending on intensity, depending on intensity. In the case of sickle hemoglobin, its formation is the result of the absence of one amino acid. Mutated hemoglobin is less liquid than typical hemoglobin and, as a result, polymers are formed in the cell. These polymers are what the individual inherits a single sickle hemoglobin gene for an individual, has a disruption of cell formation that gives him a sickle or a crescent. The amount of sickle hemoglobin present in the NOSici is usually minimal and is not enough to change the shape of red blood cells. Individuals who are carriers rarely find health problems associated with a single crescent and do not develop anemia of sickle cells.

those who inherit the sickle hemoglobin gene from both parents can only produce sickle hemoglobin, which means that a person has a sickle cell anemia. With this type of anemia, the shape of a crescent of red blood cells can inhibit blood flow, resulting in pain, increased risk of stroke and increased susceptibility to infection. Generally, the diagnosis of anemia of sickle cells is the same than the child is six months old.

symptoms of anemia of sickle cells include abdominal pain, jaundice, joint pain, fatigue, chest pain and susceptibility to infections. Symptoms can lead to episodes full of pain that can be managed by different treatment procedures. Children with anemia of sickle cellsThey become symptomatic around four months of age, so it is important that a symptomatic child can see the hematologist as soon as possible and the penicillin regime is set in the fight against infections.

bone pain is one of the most common crises experienced by people with anemia of sickle cells. In many cases, the onset of such pain crises is precipitated by an extreme change in temperature, dehydration or infection. Treatment of anemia of sickle cells include the use of antibiotics, painkillers, vitamin supplements, blood transfusions and surgery, including bone marrow transplantation. Complications such as joint inflammation, bone problems and gallbladder diseases are treated as they occur.