Hemophilia can hemophilia be cured without treating the consequences

It depends on your condition. I'm twenty-eight. The factor has only been injected once in these years.

Of course, he was rescued when he was a child. Just pay attention to yourself. I'm not ** I'm still alive.

Besides, it's just some auxiliaries. If you have money, you will suffer less, and if you don't have money, you will suffer more. It's okay.

Be strong.

Symptom. Because a person lacks a certain clotting factor in his or her plasma, when a blood vessel ruptures, the blood is less likely to clot than normal, so more blood is shed. Bleeding from wounds on the surface of the body is usually not serious, while internal bleeding is much more severe.

Internal bleeding typically occurs inside joints, tissues, and muscles. When visceral hemorrhage or intracranial hemorrhage occurs, it is often life-threatening.

Joint bleeding is common in people with hemophilia, and the most common bleeding is in the knee, elbow, and ankle joints. Blood pooling into the patient's joint space can limit joint mobility and temporarily lose function, such as when the patient is unable to stand and walk normally after bleeding from the knee. It often takes several weeks for blood to accumulate into the joint cavity to gradually be absorbed and gradually regain function, but repeated bleeding in the joint can lead to synovitis and arthritis, causing joint deformity and making it difficult for the joint to function normally, so many people with hemophilia have varying degrees of disability.

Because the genes for each clotting factor are a complex sequence, even in patients with the same type of hemophilia, the corresponding genes are different, and therefore their levels of activity of clotting factors are also different, according to which patients with hemophilia can be classified as severe, moderate, and mild.

Patients with severe hemophilia have less than 3% of the activity of clotting factors lacking in the plasma of normal people, and can bleed several times in a month, and bleeding often occurs without an obvious cause, called spontaneous bleeding. Joint bleeding is common.

Patients with moderate hemophilia have 3% to 6% of normal factor activity, and their bleeding is often caused by minor trauma, such as a sports injury. Joint bleeding usually occurs after trauma.

Patients with mild hemophilia have factor activity of 6% to 25% of the normal person, and generally bleed only after surgery, tooth extraction, or severe trauma. There is less bleeding in the joints.

Can't** Usually pay attention to timely medication at the onset of the disease No matter how good the economic conditions are, they will be affected by this disease. . . Hey, remember that no matter how difficult it is, you should take medication in time when you get sick.

Hello, if it is serious, it is not possible to lose your life, it is recommended that you still choose traditional Chinese medicine**, the cost is less, see my homepage for details.

I think it has to be **. Otherwise, a small wound is enough to kill. But it's okay to protect yourself from injury. But internal bleeding is not easy to do...

Can hemophilia be **？Hemophilia is a hereditary disorder, and prevention of hemophilia should begin before pregnancy, including genetic pulse screening. In case hemophilia is accidentally passed on to the next generation, can hemophilia be **?

Let's take a look.

Hemophilia is a lifelong bleeding disease, and prenatal examination should be carried out for carriers to control the birth of children and carriers, in order to reduce the incidence of the population and achieve eugenics.

In addition to the corresponding infusion of various coagulation factor products during bleeding, traditional Chinese medicine has a positive effect on the prevention of hemophilia and hemophilia arthritis.

1. General hemostasis**: such as the use of antifibrinolytic drugs and hemostatic drugs that generally promote platelet aggregation. For joint and muscle hematomas caused by severe bleeding, local compression such as bandages or sandbags and cold compresses can be used to stop bleeding.

2. Drugs**: The efficacy is lower than that of coagulation factor substitution**, such as the use of: desmopressin, danazol and glucocorticoids to improve vascular permeability.

3. Family**: Family** should initially be carried out under the guidance of a professional physician. In addition to injecting techniques, it also includes hematology, orthopedics, psychiatry, psychology, and prevention of HIV and viral hepatitis.

4. Surgery**: Patients with joint bleeding should be treated with fixation and physiotherapy at the same time as substitution. For patients with joint ankylosis and deformity caused by recurrent joint bleeding, arthroplasty or artificial joint replacement can be performed on the premise of supplementing sufficient coagulation factors.

5. Others**: For example, through different genes**, the patient can express a sufficient amount of coagulation factors, etc., these methods are still in the clinical trial stage and have not been fully used in clinical practice.

To prevent hemophilia, the specific content needs to be carried out according to the specific **, so that it will be more thorough, hemophilia is usually passed on to the next generation through the genetics of one parent. For example, a male hemophilia patient will pass on the hemophilia gene to all his daughters, but not to his sons. When his daughter has a child, she has a 1 in 2 chance of passing on the hemophilia gene to the child, and if she passes the gene to her son, the son will definitely have hemophilia, and if the gene is passed on to the daughter, then the daughter will still be a carrier of the hemophilia gene.

If genetic screening and identification are carried out before the couple gives birth, the culprit of hemophilia in one of the spouses can be found in advance - the disease-causing gene, and then selective pregnancy can be adopted to avoid giving birth to a hemophilia child. According to reports, since the overall prevalence of hemophilia is 100,000 in 100,000, it is not realistic to use genetic screening as a routine test method to prevent hemophilia. Experts believe that if there is a family member who is prone to bruising or frequent bleeding, it is recommended that it is best to check the hemophilia gene to avoid passing the disease on to the next generation.

Hemophilia is a relatively serious afterglow gene disease, which generally has the characteristics of family inheritance. The symptoms of hemophilia are mainly manifested in the blood, such as the patient's coagulation function is very poor, and it is generally easy to bleed, whether it is superficial bleeding or internal bleeding. So, how is hemophilia in general?

How is hemophilia inherited? What are the laws of heredity?

1. Hemostasis**

Haemostasis is the most common method for patients with hemophilia, and if the bleeding is mild, antifibrinolytic drugs and hemostatic drugs that generally promote platelet aggregation can be used. If the bleeding is severe or even causes a joint muscle hematoma, then local compression and cold compresses such as bandages or sandbags are needed to stop the bleeding.

2. Physics**

The main purpose of physical ** is to strengthen the muscles, and to accelerate their return to free movement after severe bleeding of the joints and muscles, this ** should be done immediately after severe pain, because strong muscles are effective protection for the joints.

3. Fixed**

If there is severe bleeding from the joints or muscles, it is important to immobilize the limb with some degree of splinting to prevent the diseased limb from deforming. Patients must learn how to use splints and how to use them for more time, as long shifts can cause muscle strain and joint instability.

4. Family**

If it is a family, it should be carried out under the guidance of a professional doctor, who should not only teach injection techniques, but also conduct training in the prevention of a variety of diseases, such as: hematology, orthopedics, psychiatry, psychology, AIDS, viral hepatitis, etc.

5. Surgery**

When hemophilia develops to joint bleeding, at the same time as substitution, fixation and physiotherapy should also be carried out, if the joint has repeated bleeding resulting in joint ankylosis or deformity, while supplementing sufficient coagulation factors, joint plasty or artificial joint replacement surgery should also be performed.

6. Others**

For hemophilia, in addition to the above methods, a variety of basic teasing factors can also be carried out to produce sufficient amount of coagulation silver in the patient's body, but these methods are still in a Linchuan experimental stage, and the disease is not widely used.

7. Genetic mode

1. Hemophilia A patient married a normal woman, and the son born is normal, and the daughter is a carrier.

2. If a normal man marries a female carrier, 50% of the sons born may have hemophilia A, and 50% of the daughters may be carriers.

3. The probability that a patient with hemophilia A marries a female carrier is 50% for his daughter to be a hemophilia patient and a carrier, and the probability of his son being sick is 50%.

4. A person who is a person with hemophilia who is both male and female is married, and the children born to him are all hemophilia.

Hemophilia B is inherited in a similar way to hemophilia A, with the daughters of hemophilia B being carriers and the sons being normal.

Hemophilia C is inherited in an autosomal incomplete recessive manner, which can affect both men and women, and should be considered hemophilia C if a female hemophilia patient is encountered clinically.

No, because with the continuous progress of modern science, the level is relatively mature, but there is still no specific drug, and it can only be assisted by long-term medication, as well as adjusting one's diet structure in daily life, strengthening physical exercise, etc.

At present, hemophilia is not completely **, which is a genetic disease, which is generally carried out by transfusion of coagulation factors.

There is no complete way to treat hemophilia at present, but you can't give up on yourself, once you find out that you have this disease, you should go to the hospital in time for it, and you should also pay attention to your own care, which is of great help to the disease.