AMIDEUREMETABOLISM -DISCOUNTS: CAUSES, SYMPTOMS AND TREATMENT

Deviations from amino acid metabolism with amino acid sponsorship are the most important components of proteins responsible for many and diverse operations and functions in the body. Types of amino acids are the most important types of amino acids. The following: Glycine. Glutamate. Gamma aminobutyic acid works as neuro -transfer substances. Phenylanine. Tyrosine. Tryptophan. Glycine. Each amino acid has a special and different disintegration path, and if the amino acid loses its amino group, it becomes an organic acid. Types of amino acid metabolism disorders have been identified today by dozens of enzymatic disorders in the paths of the dismaling of amino acids, some of which are acid disorders in the amino group, such as: aminoacidopathy, and the rest is organic acid, in addition to it there are many disturbances in the transfer of certain types of amino acid. One of the most famous species of the following: 1. Phenylketonuria – PKU The night of vinylketone is caused by a decrease in the activity of phenylanine hydroxillase (PAH), an enzyme that converts the amino acid phenyllanin into tyrosine, which is the cornerstone of very important hormones, skin dyes, hair and eye. Low The activity of the estate leads to the accumulation of vinyl alanine, the low amount of turquoise and other volatile. 2. Tyrosinemia (Tyrosine) leads blood to a decrease in the hydroxo acid hydroys FuhylaclacectoacetateatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatatototoTotototototototatototatototatotatotatot was allocated. to liver cancer. System, which in turn causes an imbalance in the enzyme system responsible for glyceine deviation. Symptoms of amino acid metabolism disorders The symptoms and signs differ according to the type of disorder in the amino acids, the most prominent of which are the following: 1 Symptoms of vinyl Kaiton evenings lead to ongoing high levels of vinylalanine in the blood to the following: The development of the development is gradual for the child. Small head circumference. Behavioral disorders. Patch trips. The decrease in the amount of melanin dye, which makes people with vinyl Kateon a night to own lighter formal features, such as: blonde hair and blue eyes compared to other family members who are not diseases. Not -available weight gain. Peripheral nervous diseases. Kidneys. 3.. Symptoms of a homocystein day, symptoms include the following: a clear supply in the cheeks. Long and thin structure. Lens publishing unit. Vascular disease. Bone thinner. Mental disability is formed. Psychological disorders. 4. Symptoms of lactone hypertrophy are characterized by high ketoin -ketogenic blood height with the following symptoms: attacks. Reduced muscle tension. Hickelet. Self -connection. Extreme weakness in growth. 5. Clinical signs of amino acid metabolism disorders often the clinical signs of the disease due to the accumulation of toxic intermediaries that cause certain damage, such as: phenyllelene. Phenyllactic acid. Phenyl pyrvic acid. Venylascetic acid in vinquetone. Some of these disorders are benign and harmless, such as: the presence of hysterin in the blood, due to the accumulation of a toxic intermediaries, but in most cases the method of disease is not understood. Causes and risk of risk of amino acid metabolism disorders The genetic factor is the leading cause of infection with amino acid metabolism disorders, and the inheritance of method of these diseases is considered a recessive inheritance (autosomal recessive) in most absolute. In the following, the most important mechanisms for the occurrence of the disease and its transmission are: These genetic disorders occur when parents convey the infected genes that cause disorders to their children. In most genetic metabolic disorders, both parents of the child concerned carry a copy of the abnormal gene. None of the parents usually suffer from this deviation, because there must be two copies of the abnormal gene due to the appearance of the disorder. There are some genetic metabolic disorders associated with Karomosome X (X), which means that only one copy of the abnormal gene can cause disorders in children. Complications of amino acid metabolism disorders are not thoughtful complications due to previous disorders, but the organs are the most vulnerable to the arrangement: the brain. Liver. Kidney. Not to accelerate the treatment, the previous organs can harm. Diagnosis of amino acid metabolism disorders is often detected by an amino acid concentration examination in one of the following methods: blood test. Urine analysis. Some cases also require a test to examine especially organic acids in the urine. The treatment of amino acid metabolism disorders The treatment is based on the regulation of the diet, so that foods that contain proteins and amino acids that are shared in the way of the turbulent metabolic are prohibited. Some of these disorders are investigated as part of the routine tests performed at the birth of the newborn. Of the most prominent treatment methods, depending on the type of disorder, the following: 1. Treatment of vinyl kaiton can lead to treatment with special structures and low foods of vinyllanin and protein to reduce the levels of vinylinin to the normal level and maintain normal intelligence. Rare cases of vinyl kaiton night, caused by a weak metabolism of the biopterin, which is a basic help factor in the interaction of vinylinine hydroxylase, may not be constantly responding to the treatment. 2.. Treatment of hyperrozine blood prevents treatment with nitisinon, which is a strong brake of the path of Turkuzin and thus toxic molitage. Although this medicine improves the liver, kidney and nerve symptoms, liver cancer cannot be prevented, and liver implants may be needed for acute liver disease, or in the case of cancer development. There is also a benign and short -lived form of newborns of blood turquoise that responds to the limitation of protein and vitamin C therapy. 3.. Treatment of a homocystein day that responds about 50% of people with homocysteine ​​urine for vitamin B6 treatment, and these individuals tend to have a better mental diagnosis. Beetenic treatment can be a remedy that removes excess homocystein from the body, and aspirin, and protein nutrition restriction is also useful. 4. Treatment of optical drugs of lactone lymphine that occur glyceine, such as: Dekstromethorphan, low -protein diet, and glycerine brakes, such as sodium benzoate, can relieve symptoms, but there is no treatment for this serious condition. The prevention of amino acid metabolism disorders is difficult to obtain ways to prevent infection with the infection of amino acid metabolism because it is a disease that is genetically penetrated.