1 нояб. 2005 г. · Alpha-thalassemia (α-thalassemia) has two clinically significant forms: hemoglobin Bart hydrops fetalis (Hb Bart) syndrome (caused by deletion/ ...

GeneReviews Alpha-Thalassemia - Thalassemia. Origa R, Moi P. Alpha-thalassemia. In: Adam MP, Ardinger HH, Pagon RA, et al, eds. GeneReviews. University of ...

2 дек. 2022 г. · Alpha thalassemia is a blood disorder that reduces the production of hemoglobin . Explore symptoms, inheritance, genetics of this condition.

1 мая 2023 г. · Beta thalassemia is a blood disorder that reduces the production of hemoglobin . Explore symptoms, inheritance, genetics of this condition.

Beta-thalassemia. In: Adam MP, Ardinger HH, Pagon RA, et al, eds. GeneReviews. University of Washington, Seattle. Last update Jan 2018; accessed ...

Thalassemia is an inherited blood disorder caused when the body doesn't make enough hemoglobin. Learn More

Beta-thalassemia is characterized by a reduced production of hemoglobin A (HbA, alpha-2/beta-2), which results from the reduced synthesis of beta-globin chains ...

Thalassemia comprises of a group of hemoglobinopathies, which are classified according to the specific globin chain (α or β) whose synthesis is impaired.

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. Four ...

Hemoglobin E - beta-thalassemia (HbE - BT) is a form of beta-thalassemia (see this term) that results in a mild to severe clinical presentation.