Thalassemia :
Thalassemia is a inherited anemia from parents to siblings.Patients with this disease may not experience symptoms initially , some common symptoms of thalasemia include : weakness , fatigue,deformities in facial bone , dark colored urine.Risk factors include hereditary and a family history.Parents with thalassemia can pass their genes to the children where children might also get affected with this disease.Treatment of thalasemia depends upon the severity of the disease.Bone marrow transplants, stem cell , folic acid supplementation is the treatment for thalassemia. Diagnostic test to confirm thalassemia includes complete blood picture ,gene testing, and iron studies.