Spherocytosis Support Forum

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Hereditary spherocytosis Genetic and Rare Diseases ...

    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 ...

Hereditary Spherocytosis after Splenectomy - HealthBoards

    https://www.healthboards.com/boards/anemia/445491-hereditary-spherocytosis-after-splenectomy.html
    Jan 22, 2007 · Hereditary Spherocytosis after Splenectomy Hello, my name is Jessica! I have Hereditary Spherocytosis and I have recently figured out that there is very little out there on the internet about this condition, especially support groups or places where you can talk to others about what symptoms they have with the condition.

Hereditary Spherocytosis - Home Facebook

    https://www.facebook.com/hereditarysphero
    When we hear of diabetes, epilepsy etc we all get on board so let's do the same for hereditary spherocytosis this is disease is every bit as serious and leaves some kids with no energy, immunity most of the time. Come on friends please share and help us H.S mums get our message out there we need more awareness and more help! Thank you đź’—Followers: 1.8K

Hereditary spherocytosis - Genetics Home Reference - NIH

    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.

Spherocytosis - an overview ScienceDirect Topics

    https://www.sciencedirect.com/topics/medicine-and-dentistry/spherocytosis
    Spherocytosis. Spherocytosis is one of the most common inherited hemolytic anemias. It is caused by a defect in the erythrocyte membrane, which leads to an increased permeability for sodium and water, giving the erythrocyte its typical spherical form.

Hereditary spherocytosis - Wikipedia

    https://en.wikipedia.org/wiki/Congenital_Spherocytosis
    Hereditary spherocytosis is an abnormality of red blood cells, or erythrocytes. The disorder is caused by mutations in genes relating to membrane proteins that allow for the erythrocytes to change shape. The abnormal erythrocytes are sphere-shaped (spherocytosis) rather than the normal biconcave disk shaped.Specialty: Hematology

spherocytosis DailyStrength

    https://www.dailystrength.org/group/anemia/discussion/spherocytosis
    Anemia Support Group. Anemia (or anaemia), which literally means "without blood," is a deficiency of red blood cells and/or hemoglobin. This results in a reduced ability of blood to transfer oxygen to the tissues, and this causes hypoxia; since all human cells depend on oxygen for survival, varying degrees of anemia can have a wide range of clinical consequences.

Hereditary Spherocytosis: Causes, Diagnosis, and Treatments

    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

Hereditary Spherocytosis forum Diseasemaps

    https://www.diseasemaps.org/hereditary-spherocytosis/forum/
    Hereditary Spherocytosis forum - Questions about Hereditary Spherocytosis - Ask a question and get answers from other users. Discover the new Hereditary Spherocytosis forum. Advise and help others.

Hereditary Spherocytosis (HS) Support Group Genetic and ...

    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



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