De George Syndrome: Causes, Symptoms and Treatment.

Digeorge syndrome under the protection of the George Syndrome is a condition that exists from birth, and can cause a variety of lifelong problems, including heart disorders and learning problems, and the severity of the condition vary, as some may have a serious illness that leads to death, while others can grow without realizing it. De George’s syndrome occurs because of a problem with a person’s genes called 22Q11, and the disease is usually not transmitted to the child by parents, but it can occur in some cases, and is often diagnosed shortly after birth by testing blood to check the genetic error. Each person with De George’s syndrome is affected differently and is difficult to predict the severity of the condition, as most children live to adulthood, and when they grow up, some symptoms tend, such as: heart and speech problems until they become less. However, health, behavioral, educational and spiritual problems can still affect their daily lives, and although many people with De George syndrome live to the age of adulthood, but due to health problems, they may have an average age for a little less than usual. It is therefore important to perform exams regularly to discover the problem early and can be treated. Learn the most important information on this topic in the following article: Symptoms of De George Cancer Some people do not suffer from problems, while others have some symptoms and problems, which include: 1 Symptoms of De George’s syndrome: public and include: learning and behavioral problems, including: delay in learning to walk or talk. Learning difficulties. Attention deficit disorder and hyperactivity. Autism. Speech and hearing problems, such as: temporary hearing loss due to regular ear infections. Talking slowly. With an sound -like sound. Mouth and nutritional problems, such as: a gap in the upper part of the mouth or lip. Cracked lip. Bruised palate. Problems with nutrition. Repair food through the nose. Heart problems, as some children may suffer from heart disorders from birth, including congenital heart disease. Hormone problems, and the production of a small glandular hormone, contain a dramatic neighbor’s hormone, that is, thyroid insufficiency, leading to vibration and attacks. Other problems may occur, such as: an increase in the risk of infection, such as ear infections and castles by mouth and chest infections, as the immune system is weaker than usual. Orthopedic and muscle problems, including bone pain, abnormal spinal bend, called scoliosis, and rheumatoid arthritis. Short stability, as it can be shorter than average. Mental health problems, such as: schizophrenia and anxiety disorders. 2. Other symptoms of De George Syndrome such as: Heart attack. The color of the skin changes blue. Repeated infection. A gap in the roof of the mouth. Delayed growth. Problems with breastfeeding. Not gain weight. Digestive problems. Breathing problems. Muscle weakness. The development of speech is delayed. Delay in leather. Behavioral problems. Lack of blood calcium. Endocrine system problems. Certain features, such as: uninterrupted chin, reduced ears, larger eyes or distress in the upper lip. Causes and risk factors of De George’s Syndrome occur in the George syndrome due to a problem called Limit 22Q11, and in this place a small piece of genetic substance is lost from a person’s DNA, that is, it is a deviation that occurs when a small part of the 22 chromosome lacks, resulting in a weak growth of many body systems. In about 9 of each ten cases, part of the DNA was missing in the egg or sperm that led to pregnancy, and this can happen to happen if the formation of sperm and eggs, as it is not the result of something done before or during pregnancy. In these cases, there is usually no family history of De George’s syndrome, and the risk of other children in it is often very few. Generally, about 1 in 10 cases, 22q11 was removed from a child from one of the parents with De George’s syndrome, although he may not realize that he has it when it is light. De George’s syndrome complications play parts of chromosome 22q11 a role in developing a number of body systems, and consequently De George’s syndrome can cause various errors during the growth of the fetus, which can lead to some complications, such as: heart disorders: This can lead to a lack of oxygen lichte blood supply, for example one large bowl. It comes from the heart, or a mixture of four abnormal structures for the heart. Drinka Palaceous: De George Syndrome causes smaller gear glands of natural which leads to low calcium levels and high levels of phosphorus in the blood. Ecrucular gland: In De George’s syndrome, the throat gland may be small or missing, leading to poor immune function and severe and recurring infections. Crazy Talate: Some may suffer from an opening in the mouth roof, which can lead to problems with swallowing or producing certain sounds in speech. Learning, behavior and spirit problems: Problems of the growth and function of the brain can occur, leading to learning problems or social and behavioral problems, and some can develop: attention deficit and hyperactivity. Autism -spectrum disorder. Depression. Anxiety disorders. Other mental health disorders. HIV: People suffering from the weakening of the immune system may be at increased risk for auto -immune disorders, such as: Rheumatoid arthritis. Other complications: This includes the following: Hearing impairment. Poor vision. Breathing problems. Poor kidney function. Palace stature. The diagnosis of the De George syndrome is mainly dependent on the diagnosis of the De George syndrome on a laboratory test that can remove the removal in chromosome 22Q11, and the doctor may seek this test if the child is: he has a set of problems or medical conditions that have the removal of chromosome 22. Because some defects are linked to the syndrome of the omission of chromosome 22. It is noteworthy that in some cases the child may have a set of cases indicating the omission syndrome 22q11 but the laboratory test does not indicate the removal of the chromosome 22. The doctor also through the physical examination of the face, ears, eyes and joint examination in search of any deformities. The treatment of De George’s syndrome is currently not a treatment for De George’s syndrome, as adults and children with this condition are carefully monitored to verify whether it suffers from problems, and to treat it on this basis, and this includes: hearing tests, blood testing, heart scan, length and weight measurements. Assessing their ability to develop and learn before the start of the study, as if the child is suffering from learning difficulties, it may need extra support. Speech treatment to help with speech problems and food changes. Physiotherapy for strength and movement problems. Treatment of a specialist for foot and bone problems. Use devices to evaluate bone. Tubs to improve hearing. Antibiotics to treat infections. Vitamin D supplements and calcium supplements for the Palaces Van Dergat. Psychotherapy in the case of attention deficit, hyperactivity, autism or depression. Surgery in the case of heart problems or cracked thorns. The prevention of De George’s syndrome is recommended to consult a doctor if there is a pregnancy planning and there is a family history of De George’s syndrome, whether there is a child, as the doctor may recommend a genetic test, which may include: a blood test to verify or one of the men or not. Do tests during pregnancy, such as: Take a sample of chorionic decorations or amp cells to verify if the fetus suffers from a genetic problem. The genetic diagnosis before the transplant is a type of artificial insemination, where eggs in the laboratory and the embryo test are fertilized in search of genetic problems before planting in the uterus.