A four year old girl with an angel face , but suffering from a rare disease, what is abnormal in he

Updated on healthy 2024-07-26
29 answers
  1. Anonymous users2024-02-13

    The kid is gone. In addition to the pain, the rest is also the most beautiful, that is, the parents never give up! Such a good parent, accompanied by such a well-behaved child, but the future is so miserable, that picture is really unbearable to watch.

    Go to association. It's useless to say anything. Modern medicine can't help rare genetic diseases, and others can't help them.

    The child can suffer as little as possible.

  2. Anonymous users2024-02-12

    Now the girl is receiving ** in the hospital, she is in good health and nothing unusual has happened. I hope she will have a happy childhood soon.

  3. Anonymous users2024-02-11

    This girl suffers from a neurodegenerative disease with brain iron deposition type 6 gene disease, so she still can't speak, can't take care of herself, and she may become a vegetative person in the future, which makes people feel very distressed.

  4. Anonymous users2024-02-10

    This little girl has a genetic disease because of the genetic incompatibility, which is a genetic degenerative disease of the nervous system, which is very rare, and the patient's IQ slowly recedes, and eventually it may become brain dead.

  5. Anonymous users2024-02-09

    Because of the angel face, her body has not grown, and she has been in a state of atrophy, and she can't take care of herself.

  6. Anonymous users2024-02-08

    The face cannot make normal expressions, it is inconvenient to walk, and when the situation is not good, the symptoms of hypoxia dizziness can also occur, and someone needs to be monitored at all times, and in severe cases, drugs are used to suppress the condition.

  7. Anonymous users2024-02-07

    Her disease is a hereditary neurodegenerative disease, and then after suffering from this disease, her intelligence will gradually regress and she will become vegetative.

  8. Anonymous users2024-02-06

    The body has to endure great pain every day, and because there is no medicine to take now, it is very painful.

  9. Anonymous users2024-02-05

    Is it possible for a 4-year-old angel-faced girl to suffer from a rare genetic disease? Doctor: There is no specific method.

    Recently, in Hefei, Anhui Province, a four-year-old girl named "Lan Nini" made the headlines of major reports.

    Lan Nini, who suffers from rare diseases, is very cute, with big eyes, very delicate facial features, and is also very fair-skinned, known as "Angel Face", "Silent Angel" ......

    From birth to now, Lan Nini has not been able to speak, no matter how her parents make her happy, she has no reaction, her face is expressionless.

    Lan Nini's father, spoke out on **:

    My daughter was born with a neurodegenerative disease with a type 6 gene disease of iron deposition in the brain, which has also affected her intelligence, and now she is almost five years old, she cannot speak, and she cannot take care of herself in all aspects of life. ”

    We have been giving her ** since the child was six months old, and the doctor said that the child may face regression and become vegetative in the future, but no matter what the future holds, the child's mother and I will always take care of her and accompany her to continue walking. ”

    Some netizens left a message: This little girl is as beautiful as a doll, living quietly in her own world, with ignorant eyes. There are really many rare diseases in human beings, and I hope that medicine will become better and better, and children's lives will get better and better.

    Such a beautiful child, it's really sad to look at, I hope it will be soon**.

    Doctor: There is no specific method.

    Neurodegenerative disease with cerebral ferrosis type 6 disease is due to the recessive chromosomal genes of the parents. This disease, which can be referred to as "with cerebral iron deposition", is a rare syndrome caused by chronic, recurrent subarachnoid hemorrhage or intraventricular hemorrhage, which causes hemosiderin deposition on the surface of the central nervous system. Causes of bleeding include tumors, vascular malformations, irregular postoperative scarring, or traumatic dural tears.

    This disease has a great impact on children, who cannot speak and will lose the ability to take care of themselves.

  10. Anonymous users2024-02-04

    I very much hope that this kind of Kabuhime syndrome can be **. However, the current level of global medical technology cannot be used to alleviate this disease.

  11. Anonymous users2024-02-03

    No, because such a disease is a genetic disease, it is very difficult.

  12. Anonymous users2024-02-02

    There should be no possibility of **, because genetic diseases cannot be ** according to the current level of technology.

  13. Anonymous users2024-02-01

    There is no possibility, this disease is a congenital genetic disease, and there is no way for humans to interfere with the genetic situation.

  14. Anonymous users2024-01-31

    There is no possibility of **. Because this disease is hereditary, there is no ** way yet.

  15. Anonymous users2024-01-30

    It's hard, such a disease is born, so basically there is no possibility of **.

  16. Anonymous users2024-01-29

    It is said that the possibility of ** is relatively small, but now it is already trying its best**.

  17. Anonymous users2024-01-28

    Yes, medicine is very developed now, and children are young and easy.

  18. Anonymous users2024-01-27

    In Hefei, Anhui Province, there is a four-year-old girl, very cute, very good-looking, but unfortunately because of the parents' genetic incompatibility, so this four-year-old girl suffered from a rare disease, neurodegenerative disease with cerebral iron deposition type 6 is a very rare disease, belongs to the nervous system caused by some problems, and there will be cerebral hemorrhage, vascular malformations and other symptoms, and the child who suffers from this disease, intelligence will be affected accordingly, and intelligence will slowly regress, Becoming a vegetative person generally rarely occurs this disease, and there is no way to detect it through a marriage examination before marriage.

    Generally, this situation rarely occurs, because it is rare for the genetic incompatibility of both parents to lead to this situation, and this little girl looks very cute, so the majority of netizens also expressed great distress, this neurodegenerative disease is very rare, so Chinese experts have not yet developed a way to solve this disease, can only choose to carry out some conservative **, and also to provide reasonable nutrition for the body, from many aspects to supplement the body, The girl's father was very touched when he learned that the girl was loved by everyone, and said that the girl had suffered from this rare disease since she was born, and although she was almost five years old, she could not speak.

    And in addition to the language barrier, their own life can not take care of themselves, from the time the child was born, the parents found out about this situation, began to carry out ** on her, but now there is no good ** effect, and there are doctors in related specialties said that the child may slowly regress in IQ in the future, until it becomes a vegetative person, but the girl's father said that no matter what happens in the future, they will not give up the treatment of the girl, and they will always take care of the girl.

    Because of the good health of the parents, there are now many examples of some diseases that lead to the birth of children. Therefore, slowly people will condition their bodies in advance before giving birth to children. At present, various hospitals in our country have also implemented pre-marriage, and both men and women will go to the hospital for a comprehensive examination before marriage.

    And the results of the current marriage test are required to be known to both men and women, so such an examination can largely eliminate the occurrence of many problems, but rare diseases like girls, there is no way to find out only through marriage tests or pregnancy tests, unless the DNA of the man and the woman is taken for examination, so before giving birth to a baby, you must have a comprehensive understanding of your physical health, so as to ensure that the baby can come to this world healthily.

  19. Anonymous users2024-01-26

    This little girl has a rare genetic disease, which is a hereditary neurodegenerative disease in which the mental regression of the person who suffers from this disease may eventually become vegetative. This neurodegenerative genetic disorder is rare and difficult to detect during a fetal test or premarital check-up.

  20. Anonymous users2024-01-25

    It is indeed quite rare, the probability of disease is still relatively low, this disease is also a genetic defect disease, and there is no way to solve it through **.

  21. Anonymous users2024-01-24

    It is very rare, and there have been no such cases before, and then this girl is very beautiful, but only has the IQ of a year old, and then now she is 4 years old and can't speak.

  22. Anonymous users2024-01-23

    There are very few people who suffer from this disease, and generally people who suffer from this disease will look very beautiful, but there is no solution to this disease.

  23. Anonymous users2024-01-22

    This is the first case in the world and has never been done before, so it's hard to say**.

  24. Anonymous users2024-01-21

    Recently, there is a girl with an "angel face" in Hefei, Anhui Province who suffered from a rare genetic disease, which is a hereditary neurodegenerative disease, the intelligence of the sick person will gradually decline, and finally it is likely to become a vegetative person, from the ** point of view, the girl is sweet and cute, just like an angel, I didn't expect to get this incurable disease, it is reported that it is caused by the genetic incompatibility of the parents, if there is something wrong with the girl, the parents should feel guilty and sad.

    The Angel Girl's case is distressing, the disease she suffers from is very rare, and it is difficult to detect the marriage test and the fetal test, so it cannot be avoided. It is reported that scientists need to conduct a comprehensive analysis of the genetic sequence DNA of the girl's parents in order to find out whether there are neurodegenerative genetic diseases, which are difficult to find out in ordinary physical examinations.

    The girl's father said that his daughter Lan Nini has an angel face, but she suffers from a rare disease, which has been reported by many **, and their parents are also very surprised by the child's illness. It is understood that Lan Nini has suffered from neurodegenerative genetic diseases since birth, and her intelligence has been affected, and the child is currently nearly five years old, but she can't speak and can't take care of herself, which is really pitiful.

    Lan Nini's father said that it starts when the child is six months old**, because the disease is very difficult to treat, and the child may eventually become vegetative, but they will not give up**.

    The disease that the girl suffers from is something that modern medicine can't do, and her parents can only accompany her and give her enough love, no matter what the result is, at least let the girl suffer less. **Lan Nini's eyes are pure, as if she doesn't know the difficulties she will face next, how can such a well-behaved and cute child get such a disease? I just hope she gets better and that having a healthy body is more important than anything else.

    The child is a piece of flesh that falls from the parents' body, Lan Nini's disease is caused by the genetic incompatibility of her parents, and general genetic diseases are difficult to treat, not to mention her rare genetic disease, no matter what, Lan Nini's family must go on with hope.

  25. Anonymous users2024-01-20

    On February 1, in Hefei, Anhui Province, it was reported that the four-year-old child "Lan Nini" had an angelic face. At birth, he had a genetic disorder of "neurodegenerative disease hemiencephalic iron deposition type 6".

    It is understood that the disease is relatively rare, and Nini's mother said that Nini is currently four years old and only one year old. Because of the genetic incompatibility between Nini's mother and Nini's father, the child was born with defects and his intelligence was affected. So far, she can't speak, she can't take care of herself in all aspects of life, and the doctor said that she may face regression in the future, and Nini will become a vegetative person.

    Nini's mother said she started at the age of six months. I'm almost five years old now** more than four years. The doctor said that there is no way to treat Nini's disease.

    I can only teach her more in normal times, give her more training for autistic children, and hope that she can take care of herself in the future. <>

    I believe that many netizens are like me, and they heard about genetic incompatibility for the first time. From a medical point of view, it refers to the incompatible gene body, which is often referred to as an allele, and this probability is only 1 in 10,000 in normal couples.

    1. Alleles refer to the offspring to obtain the same gene from both parents, and a pair of alleles control a certain trait, and the combination of certain two alleles will make the individual unable to survive or have low viability, which may lead to maternal infertility, ** sexual miscarriage, children will have tumors, different forms of diseases, rare diseases, strange personalities, etc. <>

    In our society that promotes eugenics, the best way to rule out a child born with a congenital disease is to have a premarital check-up. However, we do not make it mandatory. If both men and women have genetic diseases, we still recommend that the woman can do non-invasive DNA during pregnancy, which can check whether there is something wrong with the child, and do eugenics testing before pregnancy.

    We look forward to the day when we can develop a medical solution to the genetic incompatibility, so that Lan Nini can perceive the world and live independently like ordinary people. For now, Lan Nini's incident has been concerned by the majority of netizens. I'm sure Lan Nini's parents won't give up on Lan Nini's **.

    We will also continue to pay attention to let our kindness and love make Lan Nini feel happy and happy under the sun.

  26. Anonymous users2024-01-19

    The main cause of genetic diseases is caused by defects in chromosomes and genes in cells, and there are many genetic diseases that will threaten the lives of patients, and although some genetic diseases will not pose a threat to the lives of patients at birth, these diseases will gradually be revealed as patients grow.

  27. Anonymous users2024-01-18

    This is a disease caused by a genetic defect, congenital, and it's a pity that this child is really "an apple that God has bitten into".

  28. Anonymous users2024-01-17

    It is because of genes that it is congenital, and there is no way to improve it through nurture and nurture.

  29. Anonymous users2024-01-16

    A four-year-old girl in Anhui Province because her parents are genetically incompatible. As a result, little girls may be at risk of becoming vegetative, mentally degraded, and unable to take care of themselves in life.

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