Sickle-cell thalassemia beta plus with crisis with other specified complication Save

Sickle-cell thalassemia beta plus with crisis with other specified complication

Sickle-cell thalassemia beta plus with crisis with other specified complication is a genetic blood disorder. It is a type of sickle cell disease that is caused by the mutation of the beta-globin gene. This mutation causes the red blood cells to become sickle-shaped instead of the normal round shape. As a result, the sickle-shaped cells can get stuck in the blood vessels, leading to blockages and reduced blood flow to various parts of the body.

Individuals with sickle-cell thalassemia beta plus are at an increased risk of developing complications such as acute chest syndrome, stroke, and infections. The crisis associated with this condition can be triggered by a variety of factors such as dehydration, infections, and exposure to cold temperatures.

Some of the other specified complications that may occur in individuals with sickle-cell thalassemia beta plus include spleen dysfunction, bone and joint problems, and delayed growth and development. These complications can have a significant impact on the quality of life of affected individuals and may require ongoing medical care.

1. Spleen dysfunction: Individuals with sickle-cell thalassemia beta plus are at an increased risk of having their spleen not function properly. This can lead to an increased risk of infections.
2. Bone and joint problems: The reduced blood flow to various parts of the body can cause bone and joint problems, such as avascular necrosis.
3. Delayed growth and development: Children with sickle-cell thalassemia beta plus may experience delayed growth and development due to reduced oxygen supply to the body's tissues.

It is important for individuals with sickle-cell thalassemia beta plus to receive regular medical care to manage their symptoms and prevent complications. This may include regular blood transfusions, medications, and lifestyle changes such as avoiding triggers that can cause a crisis.

In conclusion, sickle-cell thalassemia beta plus with crisis with other specified complication is a genetic blood disorder that can cause a range of complications. Individuals with this condition require ongoing medical care to manage their symptoms and prevent complications.