Top 16 treatment for alpha thalassemia in 2022

Below are the best information and knowledge on the subject treatment for alpha thalassemia compiled and compiled by our own team alltopus:

1. Alpha Thalassemia

Author: www.hopkinsmedicine.org

Date Submitted: 09/04/2020 05:14 PM

Average star voting: 5 ⭐ ( 21957 reviews)

Summary: Thalassemia is an inherited blood disorder. It is passed down from one or both parents through their genes. There are two main types of thalassemia: alpha and beta. Different genes are affected for each type. Thalassemia can cause mild or severe anemia.

Match with the search results: Medicines to reduce extra iron from your body (called iron chelation therapy)…. read more

Alpha Thalassemia

2. Alpha Thalassemia

Author: www.stjude.org

Date Submitted: 10/29/2021 04:59 PM

Average star voting: 3 ⭐ ( 10895 reviews)

Summary: Alpha thalassemia is a blood disorder that reduces how well the body produces healthy red blood cells and normal hemoglobin.

Match with the search results: Deferoxamine—a liquid medicine given slowly under the skin, usually overnight, five to six nights a week, with a small, portable pump. This treatment takes time ……. read more

Alpha Thalassemia

3. Alpha-thalassemia | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program

Author: kidshealth.org

Date Submitted: 04/27/2020 04:37 AM

Average star voting: 5 ⭐ ( 46765 reviews)

Summary: A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Alpha-thalassemia

Match with the search results: Blood transfusions and chelation do not cure alpha thalassemia. Some people with alpha thalassemia major can be cured with a stem cell transplant. A stem cell ……. read more

Alpha-thalassemia | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program

4. Alpha Thalassemia Types, Diagnosis, and Treatment

Author: rarediseases.info.nih.gov

Date Submitted: 08/30/2019 01:25 AM

Average star voting: 5 ⭐ ( 93793 reviews)

Summary: Alpha thalassemia is an inherited anemia where the bone marrow has reduced production of alpha globin resulting in limited hemoglobin A.

Match with the search results: Treatment of alpha-thalassemia often includes blood transfusions to provide healthy blood cells that have normal hemoglobin….. read more

Alpha Thalassemia Types, Diagnosis, and Treatment

5. Alpha Thalassemia Treatment & Management: Approach Considerations, Iron and Folic Acid Supplementation, General Supportive Care

Author: www.verywellhealth.com

Date Submitted: 03/28/2020 08:42 PM

Average star voting: 3 ⭐ ( 37469 reviews)

Summary: The alpha thalassemia (α-thalassemia) syndromes are a group of hereditary anemias of varying clinical severity. They are characterized by reduced or absent production of 1 or more of the globin chains of which human hemoglobin is composed.

Match with the search results: No treatment is needed for people who are silent carriers (minima) or for alpha thalassemia minor. Although, people with alpha thalassemia minor ……. read more

Alpha Thalassemia Treatment & Management: Approach Considerations, Iron and Folic Acid Supplementation, General Supportive Care

6. Alpha thalassemia: MedlinePlus Genetics

Author: emedicine.medscape.com

Date Submitted: 07/25/2020 05:22 AM

Average star voting: 4 ⭐ ( 35714 reviews)

Summary: Alpha thalassemia is a blood disorder that reduces the production of hemoglobin . Explore symptoms, inheritance, genetics of this condition.

Match with the search results: Individuals with mild forms of alpha thalassemia may not require specific treatment except as needed for management of low hemoglobin levels ……. read more

Alpha thalassemia: MedlinePlus Genetics

7. Alpha Thalassemia in Children

Author: medlineplus.gov

Date Submitted: 07/03/2019 04:43 AM

Average star voting: 3 ⭐ ( 69633 reviews)

Summary: Alpha thalassemia is an inherited blood disorder. This means it is passed down through the parent’s genes. It causes anemia in affected children. Anemia is a low red blood cell or low hemoglobin level. Hemoglobin is the part of red blood cells. It carries oxygen to organs, tissues, and cells. Alpha thalassemia affects the production of hemoglobin.

Match with the search results: In people with the characteristic features of alpha thalassemia, a reduction in the amount of hemoglobin prevents enough oxygen from reaching the body’s tissues ……. read more

Alpha Thalassemia in Children

8. Alpha Thalassemia – NORD (National Organization for Rare Disorders)

Author: www.stanfordchildrens.org

Date Submitted: 12/09/2021 07:51 AM

Average star voting: 3 ⭐ ( 17126 reviews)

Summary:

Match with the search results: How is alpha thalassemia treated in a child? · A referral to a hematologist, an expert in blood disorders · Daily doses of folic acid, a vitamin vital to ……. read more

Alpha Thalassemia - NORD (National Organization for Rare Disorders)

9. Alpha Thalassemia Major

Author: www.mayoclinic.org

Date Submitted: 09/21/2019 12:12 AM

Average star voting: 5 ⭐ ( 58796 reviews)

Summary:

Match with the search results: Symptoms · Fatigue · Weakness · Pale or yellowish skin · Facial bone deformities · Slow growth · Abdominal swelling · Dark urine….. read more

Alpha Thalassemia Major

10. What is alpha thalassemia silent carrier? | Nicklaus Children’s Hospital

Author: rarediseases.org

Date Submitted: 10/18/2021 04:34 AM

Average star voting: 4 ⭐ ( 61750 reviews)

Summary: People who are alpha thalassemia silent carriers do not have the symptoms related to alpha thalassemia, such as anemia.

Match with the search results: Anemia can be associated with fatigue, weakness, shortness of breath, lightheadedness, headaches, and yellowing of the skin, mucous ……. read more

What is alpha thalassemia silent carrier? | Nicklaus Children's Hospital

11. Alpha Thalassemia – Health Encyclopedia – University of Rochester Medical Center

Author: www.cdc.gov

Date Submitted: 01/11/2021 11:32 AM

Average star voting: 4 ⭐ ( 10226 reviews)

Summary:

Match with the search results: Medicines to reduce extra iron from your body (called iron chelation therapy)…. read more

Alpha Thalassemia - Health Encyclopedia - University of Rochester Medical Center

12. Alpha Thalassemia

Author: my.clevelandclinic.org

Date Submitted: 08/08/2019 09:41 AM

Average star voting: 3 ⭐ ( 35787 reviews)

Summary:

Match with the search results: Deferoxamine—a liquid medicine given slowly under the skin, usually overnight, five to six nights a week, with a small, portable pump. This treatment takes time ……. read more

Alpha Thalassemia

13. Alpha thalassemia | Newborn Screening

Author: www.aafp.org

Date Submitted: 11/01/2021 03:16 PM

Average star voting: 4 ⭐ ( 75844 reviews)

Summary: Alpha thalassemia is an inherited (genetic) condition that affects the hemoglobin in blood. Hemoglobin is a part of your red blood cells, which carry oxygen to your body. The different types of Alpha thalassemia are:

Match with the search results: Blood transfusions and chelation do not cure alpha thalassemia. Some people with alpha thalassemia major can be cured with a stem cell transplant. A stem cell ……. read more

Alpha thalassemia | Newborn Screening

14. Thalassaemia

Author: www.hoacny.com

Date Submitted: 12/28/2019 12:56 PM

Average star voting: 5 ⭐ ( 59557 reviews)

Summary: Read about thalassaemia, a group of blood disorders that affect a substance called haemoglobin. Find out about the symptoms, causes and treatments for the condition.

Match with the search results: Treatment of alpha-thalassemia often includes blood transfusions to provide healthy blood cells that have normal hemoglobin….. read more

Thalassaemia

15. Intrauterine Therapy for Alpha Thalassemia Major: a Multidisciplinary Center – Thalassemia.com

Author: fetus.ucsf.edu

Date Submitted: 12/04/2019 02:27 AM

Average star voting: 4 ⭐ ( 93930 reviews)

Summary: Children’s Hospital Oakland and the UCSF Fetal Treatment Center’s new multidisciplinary program addresses the complex issues of families with an Alpha Thalassemia Major pregnancy. Phone: 1-800-RX-FETUS.

Match with the search results: No treatment is needed for people who are silent carriers (minima) or for alpha thalassemia minor. Although, people with alpha thalassemia minor ……. read more

Intrauterine Therapy for Alpha Thalassemia Major: a Multidisciplinary Center - Thalassemia.com

16. Alpha-thalassemia | Genetics in Medicine

Author: www.nicklauschildrens.org

Date Submitted: 07/19/2020 12:06 AM

Average star voting: 4 ⭐ ( 82490 reviews)

Summary: Alpha-thalassemia is one of the most common hemoglobin genetic abnormalities and is caused by the reduced or absent production of the alpha globin chains. Alpha-thalassemia is prevalent in tropical and subtropical world regions where malaria was and still is epidemic, but as a consequence of the recent massive population migrations, alpha-thalassemia has become a relatively common clinical problem in North America, North Europe, and Australia. Alpha-thalassemia is very heterogeneous at a clinical and molecular level. Four clinical conditions of increased severity are recognized: the silent carrier state, the alpha-thalassemia trait, the intermediate form of hemoglobin H disease, and the hemoglobin Bart hydrops fetalis syndrome that is lethal in utero or soon after birth. Alpha-thalassemia is caused most frequently by deletions involving one or both alpha globin genes and less commonly by nondeletional defects. A large number of alpha-thalassemia alleles have been described and their interaction results in the wide spectrum of hematological and clinical phenotypes. Genotype-phenotype correlation has been only partly clarified. Carriers of alpha-thalassemia do not need any treatment. Usually, patients with hemoglobin H disease are clinically well and survive without any treatment, but occasional red blood cell transfusions may be needed if the hemoglobin level suddenly drops because of hemolytic or aplastic crisis likely due to viral infections. Hemoglobin Bart hydrops fetalis syndrome currently has no effective treatment although attempts at intrauterine transfusion and hematopoietic stem cell transplantation have been made.

Match with the search results: Individuals with mild forms of alpha thalassemia may not require specific treatment except as needed for management of low hemoglobin levels ……. read more

Alpha-thalassemia | Genetics in Medicine

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