Thalassemia Topics
Topic Overview
Frequently Asked Questions
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thalassemia intermedia - person has moderate to severe anemia.
Persons with thalassemia minor have a 50/50 chance to pass the gene to their offspring, who would also have thalassemia minor.
OBJECTIVE: To determine the maternal and fetal outcomes of women complicated with thalassemia syndrome. STUDY DESIGN: Retrospective descriptive study.
Thalassemia: An inherited genetic disorder of hemoglobin in red blood cells. Most common in individuals of Mediterranean, black, or Southeast Asian ancestry.
Thalassemia: Group of inherited disorders of hemoglobin metabolism, which results in a decrease in the amount of hemoglobin formed.
Threatened abortion: Bleeding during the first trimester of pregnancy without cramping or contractions.
Beta thalassemias - Inherited anemias found mainly in people from Mediterranean countries such as Greece, Italy or Middle East countries ...
Beta Thalassemias - Inherited anemias found mostly among persons of Mediterranean and Middle Eastern descent.
BF - BreastFeed or BoyFriend.
BFN - Big Fat Negative, negative pregnancy test result.
Thalassemia is an inherited genetic condition, which your baby will only have if he inherits the gene from both you and his other parent.
It can be detected antenatally by amniocentesis or chorionic villus sampling.
thalassemia ~ a group of blood diseases, that are inherited, which affect a person's hemoglobin and cause anemia. Hemoglobin is a protein in red blood cells that carries oxygen and nutrients to cells in the body.
thalassemia - an inherited blood disorder in which the chains of the hemoglobin (a type of protein in red blood cells that carries oxygen to the tissues) molecule are abnormal; alpha thalassemia is where a mutation occurs in the alpha chain, ...
___Thalassemia
___Other chronic disease:________
Developmental Problems
___Autism
___Attention deficit/hyperactivity - a group of symptoms or signs ...
Beta Thalassemias - Inherited anemias that are most commonly found mainly in people from Mediterranean countries. The abnormality is a result of an abnormality located on chromosome 11.
α-Thalassemia-2 trait also known as Silent Carrier (α-Thalassemia-2 Trait)(One affected gene) has no consistent hematologic manifestations. The red blood cells are not microcytic, and Hb A2 and Hb F are normal.
Hemoglobin ...
Q How are thalassemias treated?
Standard treatments for patients with thalassemia major are blood transfusions, iron chelation, removal of the spleen, and bone marrow transplant.
Homozygous -thalassemia in a growth retarded, non-hydropic premature newborn
Y P M Ng, R Joseph and A Biswas
J Perinatol 28: 158-159; doi:10.1038/sj.jp.7211873 ...
"In those groups, the minor thalassemias may need more iron. But it's not recommended to give it to them routinely unless they've actually been proven to have an iron deficiency in addition to their anemia from the thalassemia," Dickerson says.
Find family genetic problems (such as Tay-Sachs disease, hemophilia, sickle cell disease, cystic fibrosis, or thalassemia) of your baby during pregnancy, especially if either you or the father has a family history of a genetic problem.
They used the method on a couple undergoing prenatal diagnosis for a type of genetic anemia called beta-thalassemia.
The risk of being a carrier of the common serious hemolytic anemia called alpha thalassemia varies, but is mostly higher than one in 10. There is also a major advantage for carriers of the thalassemias.
Preparing for pregnancy - inherited conditions
cystic; fibrosis; thalassaemia; thalassemia; genetic; pregnancy; pregnant; baby;
Talk to your doctor if you are worried about genetic (inherited) conditions such as cystic fibrosis or thalassemia.
Couples of Southeast Asian or Mediterranean origin, who are at increased risk of having children with thalassemia, a severe form of anemia.
Diseases such as sickle cell anemia or thalassemia affect the quality and number of red blood cells the body produces. If you have a disease that causes anemia, talk with your health provider about how to treat anemia.
For example, women of African or Mediterranean descent are usually tested for thalassemia or sickle cell trait or disease because they're at higher risk of these chronic blood diseases or carrying the sickle cell trait, ...
If Fifth disease occurs in the first half of pregnancy, a pregnant woman may develop anemia, a low red blood cell count that results from red blood cell destruction. Women with sickle cell disease, thalassemia or other diseases that affect red blood ...
Genetic disorders such as Tay-Sachs disease, sickle-cell anemia, and thalassemia meet these criteria, and screening tests are commonly done to identify carriers of these diseases.
Niemann-Pick Type A
Mucolipidosis Type IV
Familial Dysautonomia
Breast and Ovarian Cancer (BRCA-1 and 2) gene mutations
Thalassemia
Sickle Cell disease and other hemoglobinopathies [source: Fairfax Cryobank] ...
Mothers’ Stem Cells Could Treat Genetic Disorders Before Birth
A mother’s stem cells could potentially help battle diseases such as sickle cell anemia and thalassemia.
In most cases however, the deficiency of iron has been noted to be the cause of anemia in pregnant women. For cases of congenital anemia like thalassemia and sickle cell anemia, the situation only worsens during pregnancy.
 See also: Diagnosis, Pregnancy, Genetic, Infection, Anemia
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