Blood Diseases

Introduction:
Thalassemia is a genetic disorder of blood cells, and is described by the low level of hemoglobin and fewer red blood cells than normal, due to the emergence of symptoms of anemia fatigue and others to a lack of hemoglobin, a substance in red blood cells responsible for carrying oxygen. For More Information about Nature Review Scam

Symptoms:
Signs and symptoms depend on the type of Thalassemia and the severity of the disease, some children appear to have symptoms from birth, while others begin to appear during the first two years of age, and may not show symptoms in children with disorders in a single gene of hemoglobin.

One of the main symptoms:
A feeling of fatigue and general weakness
Shortness of breath
Pallor of the skin
Yellowing of the skin (jaundice)
Abnormalities in the bones of the face
Slow growth.

Flatulence
Change the color of urine to the dark.

Reasons:
Thalassemia occurs because of a genetic mutation in the DNA of cells consisting of hemoglobin, and this boom and transmitted genetically from parents to children.
Cause the occurrence of genetic mutations disrupt the normal production of hemoglobin, and therefore low levels of hemoglobin, and the high rate of damage to red blood cells, (which is what happens in patients with Thalassemia) lead to the emergence of symptoms of anemia.