
Sickle Cell Disease - What Is Sickle Cell Disease? - NHLBI, NIH
2024年9月30日 · Sickle cell disease affects more than 100,000 people in the United States and 8 million people worldwide. In the United States, 9 of 10 people who have sickle cell disease are of African ancestry or identify as Black: About 1 in 13 Black babies are born with sickle cell trait,meaning that they inherited a sickle cell gene from one parent.
Sickle Cell Disease - Causes and Risk Factors | NHLBI, NIH
2024年8月20日 · This child has sickle cell trait and is a carrier of the gene for hemoglobin S. A 25%, or 1 in 4, chance of inheriting two copies of the gene for hemoglobin S. This child has sickle cell disease. A child with sickle cell disease may also have one copy of the gene for hemoglobin S and one copy of a gene for another faulty hemoglobin.
Sickle Cell Disease - Symptoms | NHLBI, NIH
2024年8月20日 · Serious symptoms of sickle cell disease are emergencies and need treatment right away. Seek care or call 9-1-1 if you or someone else is experiencing: Severe pain. A serious pain event is sometimes called a “pain crisis,” “sickle cell crisis,” or “vaso-occlusive crisis.” Most people with sickle cell disease have this often-serious pain.
Sickle Cell Disease Fact Sheet - NHLBI, NIH
Sickle cell disease (SCD) is the most common inherited blood disorder in the United States. In this fact sheet, learn about the causes, signs and symptoms, diagnosis, and treatment of SCD. Print Length:
Sickle Cell Disease - Diagnosis - NHLBI, NIH
2024年9月9日 · Newborn screening programs also find out whether your baby has sickle cell trait and is a carrier of the sickle cell gene. If this is the case, genetic counseling will be offered. When a child has sickle cell trait or sickle cell disease, their future siblings or your child's future children may be a carrier of the sickle cell gene.
Sickle Cell Disease Research | NHLBI, NIH
2024年8月23日 · The Sickle Cell Genetics and Pathophysiology Lab studies the genetic and biological factors underlying the variability of sickle cell disease symptoms and complications. NHLBI scientists are using the ReFRAME Drug Repurposing Library, which lists medicines that are approved by the FDA and have the potential to treat or prevent sickle cell pain ...
Sickle Cell Disease: Research, Programs, and Progress
Sickle cell disease (SCD) is a group of painful and life-threatening genetic disorders that affect hemoglobin, the major protein that carries oxygen in red blood cells. It occurs in nearly 100,000 people in the...
Chapter 5 Hydroxyurea Therapy in the Management of Sickle Cell Disease . 31. Chapter 6 Blood Transfusion in the Management of Sickle Cell Disease . 35. Chapter 6 Blood Transfusion in the Management of Sickle Cell Disease . 35. Chapter 6 Blood Transfusion in the Management of Sickle Cell Disease . 35. Indications for Transfusion. 35
Researchers identify the high costs of living with sickle cell disease
2022年5月16日 · Potential curative therapies may help reduce the burden, but are also costly . Americans ages 64 and younger with commercial health insurance who live with sickle cell disease (SCD) pay almost four times more in out-of-pocket medical costs over their lifetimes, a total of $44,000, compared to people living without the disease.
Enfermedad de Células Falciformes (Sickle cell disease)
(Sickle cell disease (SCD) is the most common inherited blood disorder in the United States. In this fact sheet, learn about the causes, signs and symptoms, diagnosis, and treatment of SCD.) Print Length: