Lipidosis

**Lipidosis** is a polymorphic hereditary disease characterized by excessive accumulation of metabolic products of cholesterol and triglycerides, other types of lipids in various tissues of the human body, especially the nervous system, liver, spleen and other organs and leading to their damage and dysfunction. Lipidoses are the second most common group of hereditary metabolic disorders among syndromes of impaired polymer metabolism after glycogenosis.\n\nThe main manifestation of lipidosis is gradual or fulminant degenerative tissue damage with accumulation of fat of varying degrees of density. A distinction is made between fatty degeneration itself - a disease caused by asymptomatic deposition of esterified fat in tissues, and lipoidosis - diseases based on a violation of the metabolism of common

Lipidoses (also known as fat diseases) are a group of inherited disorders that are characterized by excess lipids in various organs and tissues. These disorders may be caused by genetic mutations or metabolic problems. Lipid disorders can significantly impair the quality of life of patients, causing problems with digestion, the nervous system, and other organs. Treatment for lipidosis includes drug therapy, dietary therapy, and surgery when necessary. In this article we will look at the different types of lipid disorders, their symptoms

Lipidosis is a group of genetic diseases that are associated with metabolic disorders (metabolism) of fats. Fats are called lipids and they are an important nutritional component for our body. However, with hereditary disorders of lipid metabolism, the body cannot properly break down fats and absorb nutrients from them