What does Athal mean?
What does Athal mean?
The meaning of Athal is ‘new Ireland. ‘ This name is especially approved for ‘Boys’ Gender.
What is alpha globin common mutation analysis?
Alpha-Globin Common Mutation Analysis – Alpha Thalassemia is a common hereditary trait and disease among individuals of Asian heritage. Disease ranges in severity from mild abnormalities of erythrocytic indices to severe anemia. Genetic counseling may be advised for some patients.
What is the meaning of Hemoglobin H disease?
Hemoglobin H disease (HbH) is a form of alpha thalassemia in which moderately severe anemia develops due to reduced formation of alpha globin chains. In this condition, as in the other forms of thalassemia, there is an imbalance of globin chains needed to form hemoglobin.
What are the symptoms of Hemoglobin H disease?
Hemoglobin H disease. This type causes moderate to severe symptoms. These include lack of energy (fatigue) and exercise intolerance. You may also have an enlarged liver or spleen, yellowish skin, and leg ulcers. You have a greater risk of having a child with the most severe type, alpha thalassemia major.
Is Hemoglobin H disease common?
Hemoglobin H (Hb H) disease is the most common form of thalassemia intermedia and has many features that require careful consideration in management.
What should I eat if I have alpha thalassemia?
Nutritional deficiencies are common in thalassemia. It is recommended that patients going through blood transfusion should opt for a low iron diet. Avoiding iron-fortified foods like cereal, red meat, green leafy vegetables & Vitamin C-rich foods is the best option for thalassemic patients.
Can you live with alpha thalassemia?
What are the survival rates for alpha thalassemia? Treatment for hemoglobin H has improved, and people with a moderate or severe form of the disorder are living longer with better quality of life. However, health problems caused by alpha thalassemia and its treatment are common and can be serious.
How is HbH disease diagnosed?
HbH disease should be considered in infants or children with mild-to-moderate microcytic hypochromic hemolytic anemia and hepatosplenomegaly. Heinz bodies can be detected on blood smears after cresyl blue staining. Hb biochemical analysis reveals the presence of HbH (5-30%). Diagnosis is confirmed by genetic testing.
