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Thalassaemia carriers. If you're a carrier of thalassaemia, it means you carry one of the faulty genes that cause thalassaemia, but you do not have thalassaemia yourself. Being a carrier of the trait is sometimes known as having the thalassaemia trait or having thalassaemia minor.
Jun 17, 2024 · Thalassemia is a genetic disease that reduces your body’s ability to produce healthy hemoglobin. Alpha- and beta-thalassemia disease can cause serious illness and require ongoing care, but...
Jun 3, 2022 · Thalassemia is a blood disorder that affects your body’s ability to produce hemoglobin and healthy red blood cells. Types include alpha and beta thalassemia.
Jul 10, 2024 · Thalassemia carriers typically do not experience thalassemia symptoms, but they may experience anemia symptoms, such as fatigue and skin paleness. Learn more here.
Apr 6, 2023 · If you have thalassemia trait, it means you carry a genetic mutation that causes thalassemia, but you don’t have the disease yourself. You likely won’t have any symptoms.
Nov 14, 2019 · Thalassemia is inherited, meaning that at least one of your parents must be a carrier of the disorder. It’s caused by either a genetic mutation or a deletion of certain key gene fragments.
A carrier of thalassaemia is someone who carries at least 1 of the faulty genes that causes thalassaemia, but does not have thalassaemia themselves. It's also known as having the thalassaemia trait.
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Dec 27, 2013 · A child who inherits one mutated gene is a carrier, which is sometimes called "thalassemia trait." Most carriers lead completely normal, healthy lives. A child who inherits two thalassemia trait genes - one from each parent - will have the disease.
May 1, 2023 · Beta-thalassemia minor, also called carrier or trait, is the heterozygous state that is usually asymptomatic with mild anemia. Homozygosity or compound heterozygosity for beta-thalassemia mutations cause a more severe spectrum of anemias called beta-thalassemia intermedia and beta-thalassemia major.
Thalassemia is a hemoglobinopathy that is among the most common inherited disorders of hemoglobin production. The normal adult hemoglobin molecule (Hb A) consists of 2 pairs of chains designated alpha and beta.
