Ads
related to: statistics on sickle cell disease- Safety and Side Effects
Review the Important Safety
Information for this treatment.
- Treatment Journey Video
Understand the steps
and what they entail.
- Patient Resources
See the discussion guides, FAQs,
support groups and more.
- Sign Up
Sign up today to get connected
with a Patient Educator.
- About The Therapy
Learn how this therapy may help
treat the disease. Watch the video.
- Learn How It Works
Visit the official patient site to
learn how this treatment works.
- Safety and Side Effects
Search results
Results From The WOW.Com Content Network
114,800 (2015) [8] Sickle cell disease ( SCD ), also simply called sickle cell, is a group of hemoglobin-related blood disorders typically inherited. [2] The most common type is known as sickle cell anemia. [2] It results in an abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. [2]
Hematology. Sickle cell trait describes a condition in which a person has one abnormal allele of the hemoglobin beta gene (is heterozygous ), but does not display the severe symptoms of sickle cell disease that occur in a person who has two copies of that allele (is homozygous ). Those who are heterozygous for the sickle cell allele produce ...
The Sickle Cell Disease Association of America, Inc. originated in Racine, Wisconsin. Representatives from 15 different community-based sickle cell organizations came together at Wingspread, a community center, as guest of the Johnson Foundation. There was a common belief that there was a need for national attention to sickle cell disease.
Sickle cell retinopathy. Sickle cell retinopathy can be defined as retinal changes due to blood vessel damage in the eye of a person with a background of sickle cell disease. It can likely progress to loss of vision in late stages due to vitreous hemorrhage or retinal detachment. [1] Sickle cell disease is a structural red blood cell disorder ...
She also recommended increased use of oxygen during surgery for patients with sickle-cell, since the trauma of surgery increased symptoms. The blood test she developed to detect the disease at birth became a standard test in forty U.S. states by 2010 and remains the standard in most states to this day. Administrative career
Other names. Sickle cell-β thalassemia. Specialty. Hematology. Sickle cell-beta thalassemia is an inherited blood disorder. The disease may range in severity from being relatively benign and like sickle cell trait to being similar to sickle cell disease. [1] [2]
Ads
related to: statistics on sickle cell disease