He had a blood test that showed a low blood count and low hemoglobin level. The doctor said this condition usually doesn’t give you any symptoms or lead to any problems. But she said that you shouldn’t marry anyone who also has the trait.
Can thalassemia patients marry?
Aim: With good care, patients with transfusion-dependent thalassemia major (TDTM) can reach older ages, marry and reproduce.
Can you marry someone with thalassemia minor?
YES , can get married, if only one partner is carrier there is no problem BUT if both are carrier they should undergo prenatal testing.
Can 2 people with thalassemia have a baby?
If two people who are carriers of the same type of thalassaemia have children, their children have a: 25 per cent risk of developing thalassaemia major because they inherited the thalassaemia gene from both parents.
How long do thalassemia patients live?
“Most thalassaemia patients would live up to the age of 25 to 30 years. Improved facilities will help them live up to the age of 60,” said Dr Mamata Manglani, head of pediatrics, Sion hospital.
Can thalassemia be cured?
Bone marrow and stem cell transplant from a compatible related donor is the only treatment that can cure thalassemia. It is the most effective treatment.
Can thalassemia minor skip a generation?
One missing or abnormal gene makes a child a silent alpha thalassemia carrier. Silent alpha thalassemia carriers have no signs or symptoms of the disease, but are able to pass thalassemia on to their children. Two missing or mutated genes is a condition called alpha thalassemia minor or having alpha thalassemia trait.
What should a thalassemia minor eat?
Nutrition & 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.
Is fasting required for thalassemia test?
It consists of the following blood test. Fasting is not required. Hb Chromatography by Latest HPLC method on D10 Hemoglobin System from Bio Rad, USA. For HbA2 & HbF values to rule out Thalassemia.
Is thalassemia a serious disease?
Thalassemia is an inherited blood disorder that affects the body’s ability to produce hemoglobin and red blood cells. A person with thalassemia will have too few red blood cells and too little hemoglobin, and the red blood cells may be too small. The impact can range from mild to severe and life-threatening.
What part of the body does thalassemia affect?
Thalassemia can cause bone deformities in the face and skull. People who have thalassemia may also have severe osteoporosis (brittle bones). Too much iron in your blood. This can cause damage to the heart, liver, or endocrine system (glands in the body that make hormones, like the thyroid gland and adrenal glands).
Is thalassemia linked to leukemia?
The occurrence of thalassemia with leukemia is a rare event. Voskaridou et al. report a 32 years old man with thalassemia major whose leukocytosis and thrombocytosis were gradually increased and leading to a diagnosis of chronic myelogenous leukemia .