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  2. Thalassemia - Wikipedia

    en.wikipedia.org/wiki/Thalassemia

    Other symptoms of thalassemia include bone problems, an enlarged spleen, yellowish skin, pulmonary hypertension, and dark urine. [1] Slow growth may occur in children. [1] Clinically, thalassemia is classed as Transfusion-Dependent Thalassemia (TDT) or non-Transfusion-Dependent Thalassemia (NTDT), since this determines the principal treatment ...

  3. Hemoglobinopathy - Wikipedia

    en.wikipedia.org/wiki/Hemoglobinopathy

    A subset of Hb variants can cause severe disease when inherited in the homozygous or compound heterozygous state in combination with another structural variant or a thalassemia mutation. When clinical consequences occur, they may include anemia due to hemolysis or polycythemia due to alterations in the oxygen affinity of the abnormal Hb.

  4. Beta thalassemia - Wikipedia

    en.wikipedia.org/wiki/Beta_thalassemia

    Family history and ancestry are factors that increase the risk of beta thalassemia. Depending on family history, if a person's parents or grandparents had beta thalassemia major or intermedia, there is a 75% (3 out of 4) probability (see inheritance chart at top of page) of the mutated gene being inherited by an offspring.

  5. Hemoglobin H disease - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_H_disease

    Hemoglobin H disease, also called alpha-thalassemia intermedia, is a disease affecting hemoglobin, the oxygen carrying molecule within red blood cells. It is a form of Alpha-thalassemia which most commonly occurs due to deletion of 3 out of 4 of the α-globin genes.

  6. Alpha-thalassemia - Wikipedia

    en.wikipedia.org/wiki/Alpha-thalassemia

    The condition is called alpha thalassemia trait; two α genes permit nearly normal production of red blood cells, but a mild microcytic hypochromic anemia is seen. The disease in this form can be mistaken for iron-deficiency anemia and treated inappropriately with iron. [3] [1] Alpha-thalassemia trait can exist in two forms: [1]

  7. Hemoglobin D - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_D

    Heterozygous HbD-thalassemia, which causes the symptoms of thalassemia generally with mild anemia. Heterozygous HbS-D, which gives rise to sickle cell anemia, but generally milder and slower symptoms. Homozygous HbD/HbD, which is the rarest form, but is associated with HbD disease.

  8. Transfusion-dependent anemia - Wikipedia

    en.wikipedia.org/wiki/Transfusion-dependent_anemia

    Symptoms may vary based on the severity of the condition and the most common symptom is fatigue. [3] Various diseases can lead to transfusion-dependent anemia, most notably myelodysplastic syndromes (MDS) and thalassemia. [4] [5] Due to the number of diseases that can cause transfusion-dependent anemia, diagnosing it is more complicated ...

  9. Cooley's Anemia Foundation - Wikipedia

    en.wikipedia.org/wiki/Cooley's_Anemia_Foundation

    Several thalassemia treatment centers have also received funding from the CDC as part of the Center's Prevention of Complications in Thalassemia project. The Food and Drug Administration (FDA). When a new treatment for thalassemia is submitted to the FDA for review, the Foundation makes certain that the concerns of the thalassemia community are ...