Best Doctors for Thalassemia Treatment in Hyderabad

The best doctors for thalassemia treatment in Hyderabad describe thalassemia as a blood disorder in which there is a problem with the production of hemoglobin which is essential for carrying oxygen in the blood. Thalassemia is an inherited disorder that is passed down to children from parents.

Specialists of thalassemia diseases explain that thalassemia is not passed down to children through the sex chromosomes, which means that both men and women are equally affected by the disease.

The best hematologists near you explain that depending on the severity of the thalassemia that is present, it can affect fertility, and also increase the risk of certain complications during pregnancy. Infertility and risks of pregnancy can be reduced when the individual received proper treatment and the condition is well managed.

Thalassemia specialists near you diagnose thalassemia based on symptoms, medical and family history, clinical evaluation of the symptoms and signs, and investigations such as blood tests that look for the presence of abnormal hemoglobin, and DNA analysis. Prenatal tests such as chorionic villous sampling and amniocentesis that are done before a baby is born can also predict if the child will have thalassemia and how severe it will be.

Thalassemia can be a life-threatening disease depending on the type of disease present, the severity of its symptoms, and the severity of the anemia that is present. If the condition is not properly diagnosed and managed it can lead to tissue and organ damage, and subsequent life-threatening complications.

When an individual has thalassemia there is reduced production of oxygen-carrying hemoglobin in the red blood cells, which leads to the development of anemia, iron overload, infections, bone deformities, enlargement of spleen, heart problems, growth problems, etc.

In a majority of cases when thalassemia is moderate or severe it is usually detected before a child completes the age of 2 years. In cases of thalassemia minor or thalassemia traits where there are little or no symptoms, the condition may be detected much later in life.

In thalassemia, the production of hemoglobin which is responsible for the transport of oxygen is affected. Hemoglobin is made up of alpha and beta chains, and when the production of either of these chains is affected due to the mutations, hemoglobin production is affected and greatly reduced, leading to complications that can be fatal if not treated.