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Genetic diseases when diet is particularly important
Table of Contents
1. Phenylketonuria symptoms and treatment
This enzyme is necessary for the metabolic changes of phenylalanine of one of the exogenous amino acids (delivered to the body with food). This defect results in the accumulation of the amino acid in the blood and the products of its abnormal metabolism. Since phenylocytonuria is a congenital disease, its symptoms appear as early as infancy. Initially, disorders of psychological behavior and development, hyperactivity, diarrhea, vomiting and vomiting are observed in the body because of the first five years of life.2. Galactosemia symptoms and treatment
When a newborn begins to drink its mother's milk, the first symptoms are diarrhea, vomiting, loss of appetite, excessive sleepiness or sensitivity, and lack of weight gain. It should be emphasized that the sooner the disease is diagnosed, the faster action can be taken to avoid further consequences of galactose accumulation. Galactosemia is a genetic disease resulting from a lack of enzymes that convert galactase into glucose. If the disease isn't diagnosed early, symptoms of liver failure and subsequent seizures (sepsis), constipation, heart failure and intellectual malfunction occur.3. Fructosemia symptoms and treatment
The first symptoms usually occur during an extended diet, when a child starts eating vegetables and fruits. When the disease is not treated, the development of the psychotic tract is inhibited, there may be hypoglycemia (a decrease in blood glucose levels), acne, and in severe cases, liver and kidney damage. Fructose is another disease with a genetic basis. These mainly affect the digestive system vomiting, diarrhoea, bloating. As with phenylketonuria and galactosemia, the only effective treatment method is a healthy diet.4. Translate this page to Switch Polish: Switch
In addition, fructose is present in sugar (white and cinnamon), clone syrup, juices and fruit products. Therefore, sweets, sweetened beverages, alcohol and certain types of baked goods should be eliminated from the diet. It is recommended to consume meat, fish, milk and milk, eggs, vegetable fats and cereal products. It must be completely excluded from the diets of sick people. It also contains products that contain glucose-fructose syrup. It should be noted the composition of dietary supplements and lectins (especially cereals, lectin syrups, tablets for breastfeeding).5. Mycobacteriosis symptoms and treatment
In the digestive system, there is a blockage of the flow of pancreatic enzymes, which impedes the digestion and absorption of nutrients. Mucosacidosis is also associated with infertility. In women, obstructed pregnancy may be associated with menstrual disorders and excessive mucus deposition in the ovaries and cervix (which can be a barrier to sperm). Mucosa is incurable. In order to reduce inflammation in the respiratory tract, uterine excretion therapy is also performed, as well as the disclosure of sleeping medicines.6. See also the Polish Diet
This is due to impaired digestion and absorption, as well as increased breathing and coughing effort. Therefore, a high-calorie diet is the main rule of nutrition in mucosal acidosis. It is also important to supply protein the need for protein in children with mucocidosis is about 2.5 g/kg of body weight. Due to reduced absorption of fat, constant supplementation of vitamin A, D, E and K is required. The goal of nutritional mucosis is to maintain proper body weight and prevent malnutrition.
