Sickle-cell trait digital illustration

Sickle-cell trait Save


ICD-10 code: D57.3

Disease category: D57.3: Sickle-cell trait

Sickle-Cell Trait: What You Need to Know

Sickle-cell trait (SCT) is an inherited blood disorder that affects millions of people worldwide. It is caused by a mutation in the hemoglobin gene, which leads to the production of abnormal hemoglobin. While SCT carriers do not have sickle-cell disease, they can still experience health complications.

  1. Symptoms: Most people with SCT do not experience any symptoms. However, in rare cases, they may experience complications such as pain, swelling, and fatigue.
  2. Diagnosis: SCT can be detected through a simple blood test. It is important to get tested if you have a family history of sickle-cell disease or if you are planning to have children.
  3. Risks: SCT carriers are at a higher risk of developing certain health complications such as exercise-related sudden death, kidney problems, and blood clots.
  4. Prevention: There is no cure for SCT, but there are ways to prevent complications. It is important to stay hydrated, avoid extreme temperatures, and avoid situations that may cause oxygen deprivation.

It is also important for SCT carriers to inform their healthcare providers about their condition, especially before undergoing surgery or medical procedures.

Overall, while SCT carriers may not have sickle-cell disease, they still need to be aware of the risks and take necessary precautions to prevent complications.

Treatment of Sickle-cell trait:

Sickle-cell Trait: Treatment Options
Sickle-cell trait is an inherited condition that affects the shape of red blood cells. People with sickle-cell trait have a different form of hemoglobin, the protein in red blood cells that carries oxygen throughout the body. Sickle-cell trait is usually a benign condition, but it can cause some health problems. Here are some treatment options for ...

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