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Sickle cell disease is a group of blood disorders inherited from both parents, causing abnormal red blood cells that can lead to pain, anemia, infections, and organ damage. Learn about the symptoms, diagnosis, treatment, and prevention of sickle cell disease and its subtypes.
Learn about a benign condition that causes increased fetal hemoglobin production in adults, and how it affects sickle cell disease and other hemoglobin disorders. Find out the causes, diagnosis, epidemiology and references of this genetic variation.
Hemoglobin Lepore syndrome is a rare genetic disorder that causes abnormal hemoglobin production. It has three varieties: Washington, Baltimore and Hollandia, which differ in their distribution and severity.
In patients with sickle cell disease, red blood cells, which are usually disk-shaped, take on a crescent or sickle shape. This change can cause cells to clump together, leading to clots and ...
For people living with the disease, a sickle cell crisis can happen at any time. When it does, their rigid, sickle-shaped red blood cells become stuck in their blood vessels, blocking flow and ...
Graham Roger Serjeant CMG (born 1938) is a British medical researcher who studied sickle-cell disease in Jamaica, setting up screening programmes and a cohort study from birth. He directed the MRC Laboratories at the University of the West Indies and instituted the Sickle Cell Trust (Jamaica), a local charity. He has written four books and ...
The Epidemiology Data Center is located at 4420 Bayard Street, Suite 600, Pittsburgh, PA 15260. ... SCD-CARRE – Sickle Cell Disease and CardiovAscular Risk ...
A rare inherited blood disorder caused by a sickle cell allele and a beta thalassemia allele. Learn about the signs, symptoms, diagnosis, treatment, and mutations of this disease.
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