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Diseases Details

Thalassaemia [View testimonials]
 Thalassaemia is a anaemic blood disorder. A person suffering from this disorder has defective manufacture of hemoglobin and ineffective erythropoiesis ie. manufacture of blood cells in the bone marrow. Thalassaemia is one of the most common inherited disease.This disorder is geographically common in the people of Mediterranean, African and Southeast Asian origin. The cause of the disease is not known other than the fact that it is an inherited disorder.

Thalassaemia can be ß-Thalassaemia, and alpha-thalassaemia. These can be further broken into major and minor thalassaemia.
Thalassaemia Major is the severe type where the patient has acute anaemia. The patient has frequent leg ulcers, enlarged spleen and jaundice. Ineffective erythropoiesis causes abnormal skeletal development. The long bones suffer frequent fractures and growth is stunted. Iron deposits in the heart muscles can cause complications and heart failure. Iron deposits in liver lead to dysfunctioning of the liver. The life expectancy of Thalassaemia patients is greatly diminished.

Thalassaemia Minor patients have slight anaemia but lead normal lives. Such patients at times do not even know they are carrying the disease. It is discovered only after a special blood test. Sometimes a Thalassaemia Minor patient discovers the disease after his/her child has Thalassaemia Major. Therefore it is of prime importance to know if you have Thalassaemia Minor when you want to start a family.

Symptoms:
 

Signs and symptoms of thalassemias are due to lack of oxygen in the bloodstream. This occurs because the body doesn''t make enough healthy red blood cells and hemoglobin. The severity of symptoms depends on the severity of the disorder.

No Symptoms

Alpha thalassemia silent carriers generally have no signs or symptoms of the disorder. This is because the lack of alpha globin protein is so small that hemoglobin works normally.

Mild Anemia

People who have alpha or beta thalassemia trait can have mild anemia. However, many people with this type of thalassemia have no signs or symptoms.

Mild anemia can make you feel tired. It''s often mistaken for iron-deficiency anemia.

Mild to Moderate Anemia

People with beta thalassemia intermedia have mild to moderate anemia. They also may have other health problems, such as:

  • Slowed growth and delayed puberty. Anemia can slow down a child''s growth and development.
  • Bone problems. Thalassemia may make bone marrow (the spongy material inside bones that makes blood cells) expand. This causes wider bones than normal. Bones also may be brittle and break easily.
  • An enlarged spleen. The spleen is an organ that helps your body fight infection and remove unwanted material. When a person has a thalassemia, the spleen has to work very hard. As a result, the spleen becomes larger than normal. This makes anemia worse. If the spleen becomes too large, it must be removed.

Severe Anemia

People with hemoglobin H disease or beta thalassemia major (also called Cooley''s anemia) have severe thalassemia. Signs and symptoms occur within the first 2 years of life. They may include severe anemia and other serious health problems, such as:

  • Pale and listless appearance
  • Poor appetite
  • Dark urine
  • Slowed growth and delayed puberty
  • Jaundice (a yellowish color of the skin or whites of the eyes)
  • Enlarged spleen, liver, and heart
  • Bone problems (especially bones in the face)
  • Paleness
  • Headaches
  • Fatigue
  • Shortness of breath
  • Jaundice
  • Spleen enlargement

Stem Cell Therapy:
Now, such incurable diseases can be treated by Stem Cell Therapy.

Where Stem cells are being taken from patient’s own bone marrow, Adipose derived fat stem cells, peripheral blood derived stem cells or Umbilical cord blood-derived & placenta-derived immune rejection free stem cells. No. of experts in different parts of the world say Germany, Mexico, Ukraine, India, China and many more have treated thousands of patients suffering from incurable disease improving their Life quality.

To get your medical condition evaluated by this global medical experts team & to contact experienced patients in this regard, contact SCGF or become its member.

 
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