There is a rare disease called self destructive disfigurement syndrome, which is 1 in 380,000, what

Updated on society 2024-07-26
4 answers
  1. Anonymous users2024-02-13

    Self-disfiguring syndrome is a condition in which the loss of guanine and hypoxanthines causes excess uric acid in the body, causing changes in the face. This disease is mostly caused by genetic defects, which is difficult to carry out through scientific means**, and patients can only endure the pain of this disease, allowing themselves to bear a series of pains caused by the destruction of their appearance, such as bearing the blame and ridicule of others, and making their lives and work face problems. <>

    Cells produce free bases and nucleosides when they are renewed, and these two components require less energy to be synthesized and remedied, but they are important parts of bone marrow, platelets, leukocyte brain, etc., so the importance of these two substances to the human body can be imagined. If the human body lacks these factors, there will be serious genetic defects, leading to the appearance of self-destructive appearance signs, such as mental retardation, brain dysplasia and other diseases that need family members to worry about. <>

    In addition, free bases and nucleosides will synthesize purines, and if the purines in the human body cannot be converted, it will increase uric acid, and the content of uric acid will cause purines to produce a closed cycle when decomposing, which will increase the burden that the human body needs to bear. When the limit is exceeded, people with self-destructive disfigurement syndrome bite their hands, feet, and lips without being conscious. <>

    This disease runs in families, and once a man develops the disease, all males of his family descendants may inherit the disease, which is known as lineage-linked recessive inheritance. In order to prevent the increase of uric acid, the cause of this kind of disease must be symptomatic**, once abandoned**, then it is difficult for the patient to successfully live to the age of 10 years. If the medication is inappropriate or the condition is more serious, it is difficult for the child to live to adulthood in the case of **.

    Therefore, it is necessary to do relevant examinations for the child at the time, and only the normal indicators of the disease, or the timely detection of the condition prematurely, can make the child less prone to this disease.

  2. Anonymous users2024-02-12

    Patients become uglier and less confident about their appearance, and they tend to gain weight.

  3. Anonymous users2024-02-11

    Patients may have extreme low self-esteem, and then they will cause some damage to their appearance, and feel that they are not as good as others.

  4. Anonymous users2024-02-10

    The patient's face will be disfigured, and it will not live up to the appearance of a normal person. We should pay attention to the changes in our body in time and go to the hospital regularly for physical examinations.

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