Does thalassemia cause heart failure5

Thalassemia will definitely lead to heart failure for a long time, and the key is to replenish a large amount of qi and blood energy in the body to achieve remedy. The only effective way to do this is to sleep between 6-12 p.m.

Because this time period is the only effective sleep period for the body to replenish qi and blood energy, only in this period of sleep can the replenishment of qi and blood energy, normal people need to sleep 70 minutes a day in this time period to achieve energy balance, if the sleep time in this time period is greater than 70 minutes every day, then the body replenishes the qi and blood energy is superfluous, and the excess energy can be used to repair the body's ischemic state, the more time you sleep during this time period, The more energy your body replenishes, the faster it recovers, and the faster your body recovers.

If the sleep time is less during this period, the less energy the body replenishes, and it is difficult for the body to repair itself, which is very likely to lead to heart failure. Either way, it is advisable to go to bed early to solve the problem.

Severe anemia can eventually lead to heart failure.

1. Longan lotus seed soup: Method: Add 20 longan and 50 lotus seeds, add an appropriate amount of water, and cook until the lotus seeds are soft and ripe. Function: strengthen the spleen, calm the nerves, nourish blood.

2. Longan porridge: Method: 15 grams of longan meat, 10 red dates, and 50 grams of japonica rice, and boil them into porridge. Function: nourish the heart and spleen, most suitable for people with anemia and insomnia and forgetfulness.

In addition, insisting on making a cup of Xueying tea every day can play a role in replenishing qi and blood, strengthening the spleen and helping digestion, replenishing stagnation, and achieving the purpose of comprehensively regulating anemia.

The harm of thalassemia to the human bodycopy:bai

1) Severe: Anemia, progressive aggravation of hepatosplenomegaly, jaundice, and dysplasia occur within a few days of birth, and its special manifestations are: large head, widening of the eye distance, saddle nose, forehead protrusion, cheek protrusion, its typical manifestation is a buttock-like head, long bones can be fractured.

Skeletal changes are caused by hyperhematopoiesis of the bone marrow, widening of the bone marrow cavity, and thinning of the cortex. A small number of patients develop a thoracic mass between the ribs and spine, and gallstones and leg ulcers may also be seen. Common complications include acute pericarditis, secondary hypersplenism, and secondary hemochromatosis.

2) Intermediate: mild to moderate anemia, most patients can survive to adulthood.

3) Mild: mild anemia or asymptomatic, generally found during the investigation of family history.

People with anemia can drink Guxue tea to regulate qi and blood, nourish yin and nourish blood and moisten dryness.

The molecular structure and synthesis of globin chains are determined by genes. , and globin genes to form a "gene family", and globin to form a "gene family". Normal people inherit 2 globin genes from each parent ( ) to synthesize enough globin chains; Inherit 1 globin gene from each parent to synthesize enough globin chains.

Due to the deletion or point mutation of the globin gene, the peptide chain synthesis disorder leads to the disease. Thalassemia is divided into four types: type, type, type δ and type δ, among which thalassemia is more common.

1.The molecular pathology of globin dyspoietic anemia (thalassaemia) is quite complex, and more than 100 gene mutations are known, mainly due to point mutations in genes, and a few are gene deletions.

2.Globin dysgenesis anemia (thalassemia)Most globin dysgenesis anemia (thalassemia) is caused by a loss of the globin gene, and a few are caused by point mutations. It is caused by the deletion of the white gene, and a few are caused by point mutations.

The anemia we refer to is basically iron deficiency anemia, what is this anemia and what causes it? Iron deficiency anemia is a type of microcytic hypochromic anemia caused by insufficient iron stores in the body, which affects hemoglobin synthesis. Iron deficiency anemia can be caused by many causes, such as malnutrition, iron deficiency, iron malabsorption, and chronic or acute blood loss.

Pairing two cups of Depu Guxue and tea every day is a good way to regulate and improve the symptoms of qi and blood deficiency.

What's going on with anemia:

Anemia can cause low hemoglobin, resulting in a decrease in the ability of hemoglobin to carry oxygen, due to insufficient oxygen supply, more blood flow in the body to important organs, and those organs that have little temporary impact, such as **, mucous membranes, etc., blood vessels begin to contract. As a result, there is often whitening of the mucous membrane in the eyelids. This phenomenon is especially noticeable on parts of the lips, nails, and earlobes.

Unable to supply enough oxygen to the cells, the body suffers from shortness of breath, rapid heartbeat, fatigue, fatigue, loss of appetite, and drowsiness. In addition, it is easy to cause hypoxia in the brain, affect normal thinking, make thinking ability worse, forgetfulness, and often appear dizzy, dizzy, tinnitus, etc.

Cause of anemia 1:

Iron is an important trace element in hematopoiesis, and dietary iron deficiency is the main cause of anemia. Malnutrition anemia mainly refers to severe iron deficiency in the body, followed by anemia caused by lack of vitamin B12, especially the lack of iron, protein, vitamin B12 and other hematopoietic raw materials in the body caused by picky eating.

Cause 2 of anemia:

Iron deficiency anemia can also be caused by iron malabsorption or loss of iron, such as hookworm infection, gastrointestinal malabsorption, bleeding from gastric and duodenal ulcer disease, hemorrhoidal bleeding, menorrhagia in women, and functional uterine bleeding during puberty.

Cause 3 of anemia:

Blood loss is the most common cause of anemia and can be divided into acute and chronic. Chronic blood loss often causes iron deficiency anemia; Anemia caused by massive blood loss in a short period of time due to rupture of blood vessels or defects in hemostasis mechanisms due to trauma or disease processes is called acute hemorrhagic anemia.

Thalassemia, also known as marine anemia, is a congenital blood disorder that is genetically related to parents. The patient's red blood cells are fragile and prone to death, and their oxygen-carrying capacity is insufficient, and they are unable to live normally beyond certain degrees. Before marriage, health check-ups can be screened out, which is a recessive gene inheritance, and the size of red blood cells in patients is smaller than normal cells, and sometimes they are pale or targeted due to low heme content. Thalassemia can be recessive, mild, and severe.

Thalassemia is caused by the abnormal structure of globin in human blood, which is a genetic inheritance disease, with a genetic tendency and a certain regionality, such as Fujian, southern Fujian and other regions with a high incidence. Therefore, the disease has a genetic predisposition, so women who are preparing to conceive or women who are already pregnant should go to a regular hospital for examination as soon as possible, especially when they are found to have anemia symptoms, they should pay more attention to screening for thalassemia, so as not to pass on the problematic genetic defects to the next generation.

Hello! Please don't worry too much, you have no symptoms, and you have recently donated blood to qualify, indicating that the so-called "thalassemia" detected in your marriage examination should be a thalassemia gene carrier, which has no impact on your health. However, if your subject happens to be a carrier of the same type of thalassemia (both are gene carriers, or both are gene carriers), there is a 1 4 (or 25%) chance of developing moderate to moderate or major thalassemia in the future, and such children will need frequent blood transfusions and iron removal agents, which will put a great burden on the family.

It is recommended that you do thalassemia gene testing first, and after determining which gene carrier it is, your subject should also be tested for the same thalassemia gene, if only you have it, and the subject does not, it doesn't matter. If both partners carry the same gene, by the third month of pregnancy, prenatal diagnosis should be done, and the fetus will have an abortion if it is moderate or major thalassemia.

In addition, to add that your parents do not have thalassemia, it only means that they are also thalassemia gene carriers, have no symptoms, and have not been to the hospital for check-ups, so they do not know.