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https://www.diseaseinfosearch.org/organization/view/131
Jan 03, 2019 · Are you looking for disease information or support? Simply type in the name of a disease or condition and Disease InfoSearch will locate quality information from a database of more than 13,000 diseases and thousands of support groups and foundations. ... Hereditary Spherocytosis (HS) Support Group Disease Support Organization. Last ...
https://ghr.nlm.nih.gov/condition/hereditary-spherocytosis
Oct 15, 2019 · Hereditary spherocytosis is a condition that affects red blood cells. People with this condition typically experience a shortage of red blood cells (anemia), yellowing of the eyes and skin (jaundice), and an enlarged spleen (splenomegaly).Most newborns with hereditary spherocytosis have severe anemia, although it improves after the first year of life.
https://rarediseases.info.nih.gov/diseases/6639/hereditary-spherocytosis
Jun 19, 2018 · Hereditary spherocytosis is a condition characterized by hemolytic anemia (when red blood cells are destroyed earlier than normal). Signs and symptoms can range from mild to severe and may include pale skin, fatigue, anemia, jaundice, gallstones, and/or enlargement of the spleen. Other symptoms of hemolytic anemia may include feeling that your heart is pounding or racing (palpitations ...
https://www.ncbi.nlm.nih.gov/books/NBK539797/
Hereditary spherocytosis (HS) is the most prevalent cause of hemolytic anemia due to an abnormal red cell membrane and classifies as a type of congenital hemolytic anemia. Oskar Minkowsky first described it in the early 1900s.[1] Erythrocytes are unable to maintain their normal biconcave shape due to genetic mutations in membrane/cytoskeletal proteins that play a role in structural morphologic ...
https://www.cancertherapyadvisor.com/home/decision-support-in-medicine/hematology/hereditary-spherocytosis/
Hereditary spherocytosis typically presents in infancy or childhood but may present at any age. In children, anemia is the most frequent finding (50%), followed by splenomegaly, jaundice, or a ...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2975852/
Hereditary spherocytosis (HS) is a familial haemolytic disorder with marked heterogeneity. Clinical features range from asymptomatic to fulminant haemolytic anaemia. …
https://rarediseases.info.nih.gov/organizations/169
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https://www.healthline.com/health/congenital-spherocytic-anemia
Hereditary spherocytosis is a disorder of the red blood cell membrane that causes the cells to be spherical rather than flat. Learn complications and more.Author: Carmella Wint
https://www.uptodate.com/contents/hereditary-spherocytosis
Although relatively rare, hereditary spherocytosis (HS) is the most common cause of hemolytic anemia due to a red cell membrane defect. It is a result of heterogeneous alterations in one of five genes that encode red blood cell (RBC) membrane proteins involved in vertical associations that link the membrane cytoskeleton to the lipid bilayer.
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