Family Independent Functional: Symptoms, Causes and Treatment

Family dysautulomy, under the protection of the dysfunction of the independent function of the family, is a genetic disease, physical, physical, caring that affects the involuntary, sensual and motor nervous system, which greatly harms the performance of many devices in the body. There is a 25% possibility in every pregnancy that the parents who carry the disease have a child with an injured child, and a 50% possibility that the gene is inherited for their healthy child, as many antenatal and recording checks are recently performed to seek and identify patients and no containers. There was significant progress in 2001 with the creation of the gene that disruption of the family -independent functions in the chromosome no. 9 caused, and 3 mutations were found in the gene (IKB cap), where the basic boom affects 99.5% of cases on the composition of the gene, and thus produces a shorter protein than usual. Patients with family independent functions produce healthy protein in addition to short proteins in different relationships in different tissues, while the second mutation is associated with the basic mutation and leads to an amino acid. Symptoms of family -independent functional fects show symptoms in different degrees of danger between patients and the same patient at different ages, and the most important symptoms include the following: a lack of tears. Eating problems, especially in babies, where breastfeeding is low. Hashah if it swallows. Food inhalation. Lung fluids. A visual integral reflux. Burn. Stomach pain. Vomiting. Breathing problems. Repeated pneumonia. Problems and stop breathing when you cry and sleep. High blood pressure. sweat. Red leather stains. The rise of episodes in cases of physical ordeal or psychological emotion. Faint and attacks. Archive behind. Fractures. Delayed growth. Increase in weight and length. Causes and factors of the risk of disruption of the independent function of the family in the following clarification of the causes and risk factors: 1. The causes of infection with the disruption of the independent family function the mutations in the gene cause a defect in the family balance as the gene provides a protein instructions in a variety of cells in the body. Almost all individuals with family speech defect have two copies of the same genetic mutation in each cell, as this mutation can disrupt how information is collected in a gene to make a protein production scheme. Due to this error, a reduced amount of natural protein is produced, but this mutation carries it in an inconsistent way and some cells produce amounts near natural protein, while other cells, especially brain cells, contain very little protein. Critical activities in the brain cells are likely to be disrupted due to low or lack of protein quantities, leading to signs and symptoms of family weather error. 2. Risk factors infection with the disruption of the independent family function includes the most important risk factors infection with the following: diabetes. Parkinson’s disease. Muscle stiffness. Rheumatoid arthritis. SL. Sarkoid. Crohn’s disease and ulcerative colitis. Digestive disorders. Guilllain-Barre syndrome. Lambert-Aaton syndrome. Vitamin B deficiency and vitamin E. HIV. Lyme disease. Complications of family -independent function defects The complications of family -independent function disorder vary depending on the symptoms they suffer from. In severe cases, people can suffer from life -threatening complications, such as: pneumonia and breathing failure. The most important complications include the following: abnormal heartbeat. faint. Breathing problem. Digestive problems. Visual problems, such as: vague vision. Diagnosis of family -independent functional function is diagnosed based on the following: Clinical symptoms in physical examination, which include: the presence of a little taste of taste. Saliva. Muscle bag. Low or fully lost string reactions. A decrease in the sensitivity of the cornea. Changes with feelings of pain, heat and cold. Walking is wrong. Skin examination of histamine. Genetic investigation. Family independent function -defect treatment includes the most important treatment methods as follows: Family -independent function -defect treatment focuses on relieving symptoms. Treatment options include medicine to control blood pressure, breathing problems and vomit attacks. Some people suffering from dysfunction of the family’s independent function need a dietary tube due to swallowing problems. Some people need surgery to correct the curvature of the spine. Prevention of the independent functional dysfunction of the family The genetic DNA test is very accurate for determining the occurrence of family -independent functional disease as it can be used to diagnose people with this condition or those who carry the gene, and it can also be used to prevent prenatal diagnosis.