Searching for Spherocytosis Support information? Find all needed info by using official links provided below.
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.
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://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://www.primehealthchannel.com/spherocytosis.html
May 22, 2013 · Spherocytosis Support Groups. Patients and their family members can seek assistance and necessary information from various support groups that provide guidance to Spherocytosis sufferers. The support groups also include a number of online forums that have recently come into existence. Spherocytosis Pictures
https://rarediseases.info.nih.gov/organizations/169
If you have problems viewing PDF files, download the latest version of Adobe Reader. For language access assistance, contact the NCATS Public Information Officer. Genetic and Rare Diseases Information Center (GARD) - PO Box 8126, Gaithersburg, MD 20898-8126 - Toll-free: 1-888-205-2311
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://en.wikipedia.org/wiki/Spherocyte
Spherocytosis is the presence in the blood of spherocytes, i.e erythrocytes (red blood cells) that are sphere-shaped rather than bi-concave disk shaped as normal.Spherocytes are found in all hemolytic anemias to some degree. Hereditary spherocytosis and autoimmune hemolytic anemia are characterized by having only spherocytes.Specialty: Hematology
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.
https://www.uptodate.com/contents/hereditary-spherocytosis/print#!
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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