The characteristics and risk factors of sickle cell anemia

This can help you understand possible treatments, preventive measures, and reproductive options. For the transplant to work, the bone marrow must be a close match.

Risk Factors for Sickle Cell Anemia

Fever frequently is associated with the pain crises. It can lead to impotence if left untreated.

Sickle Cell Disease (Sickle Cell Anemia)

Eye Damage The critical area of the eye that normally senses light is called the retina. The impaired circulation is caused by the blockage of various blood vessels from the sickling of red blood cells.

These patients can develop shock and lose consciousness. Typically, the site of red blood cell production bone marrow works overtime to produce these cells rapidly, attempting to compensate for their destruction in the circulation. There also are a few rare types of SCD: Repeated pulmonary infarcts can lead to scarring of the lungs of children with sickle cell anemia by the time they reach adolescence.

Painful bone infarcts can be relieved by rest and pain medications. Diagnosis SCD is diagnosed with a simple blood test. After early diagnosis, the goal is health maintenance to prevent complications and medicines and treatments to manage complications, including chronic pain.

Environmental determinants of severity in sickle cell disease

These possibilities should be discussed with the primary care doctor, a blood specialist called a hematologist, or a genetic counselor. Swelling in the hands or feet.

Sickle cells can block tiny blood vessels that supply your eyes. Infections of the lungs require aggressive antibiotics. Some experts will prescribe hydroxyurea to people with other types of sickle cell disease who have severe, recurrent pain.

In this review, we have not considered the effects of infections, including malaria, as this is a very large area and is the subject of several recent reviews.

Materials and methods We analyzed individuals with a diagnosis of sickle cell anemia Hb SS between the ages of 11 and 30 years old, receiving routine medical care at the University of Ibadan, Ibadan, Oyo, Nigeria and individuals with sickle cell anemia between the ages of 11 and 30 years old, receiving routine medical care at UIC, Chicago, IL, USA.

What is Sickle Cell Disease?

Both your parents need to pass the abnormal hemoglobin gene on to you in order for you to develop the disease.Anemia (looking pale) Dark urine If you have any of these risk factors along with signs and symptoms of sickle cell anemia, it’s important to visit your physician right away so that you can get started on a treatment plan.

Our findings are consistent with the possibility that higher values for BMI and BP in Chicago sickle cell anemia patients may contribute to an increased risk of stroke and highlights the need for measures to reduce these risk factors.

This is commonly called sickle cell anemia and is usually the most severe form of the disease. HbSC People who have this form of SCD inherit a sickle cell gene (“S”) from one parent and from the other parent a gene for an abnormal hemoglobin called “C”.

Risk factors. For a baby to be born with sickle cell anemia, both parents must carry a sickle cell gene. In the United States, it most commonly affects black people.

Complications. Sickle cell anemia can lead to a host of complications, including: Stroke. A stroke can occur if sickle cells block blood flow to an area of your brain. Sickle cell anemia, or sickle cell disease (SCD), is a genetic disease of the red blood cells (RBCs).

American Society of Hematology

Normally, RBCs are shaped like discs, which gives them the flexibility to travel through even the smallest blood vessels. Sickle cell anemia is a genetic condition present from birth, with symptoms usually beginning to appear at about 4 months old.

The main symptom of the condition is low red blood cell count, a form of anemia, which often causes pale skin and nails.

The characteristics and risk factors of sickle cell anemia
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