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Hb-SS disease is a genetic disorder that affects the production of hemoglobin in the body. This disease is also known as sickle cell anemia. People with Hb-SS disease have abnormal hemoglobin that causes red blood cells to become sickle-shaped instead of round. These sickle-shaped cells can get stuck in small blood vessels, leading to pain and other complications.
One of the most common complications of Hb-SS disease is a crisis. A crisis occurs when there is a sudden increase in the number of sickle-shaped cells in the blood. This can cause severe pain in the bones, joints, and chest. Other symptoms of a crisis may include fever, swelling, and difficulty breathing.
In addition to crises, people with Hb-SS disease may also experience other complications. These can include:
Managing Hb-SS disease with crises and other complications can be challenging. However, there are treatments available that can help alleviate symptoms and prevent further complications. These treatments may include blood transfusions, medications, and lifestyle changes such as avoiding triggers that can lead to crises.
If you or someone you know has Hb-SS disease, it is important to work closely with a healthcare provider to manage symptoms and prevent complications. With proper management, people with Hb-SS disease can live long and healthy lives.
Hb-SS disease with crisis and other specified complications is a serious genetic disorder that affects the production of hemoglobin in the body. The disease is also known as sickle cell anemia, and it can cause severe pain, organ damage, and other complications. While there is no cure for Hb-SS diseas...
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