Storage Diseases

Storage diseases are a group of genetically determined diseases associated with metabolic disorders that cause the accumulation of various substances in tissues and cells - mucopolysaccharides, glycoproteins, metals, acids or their metabolites. Hereditary diseases of this group are among the most common hereditary diseases in children.

Storage diseases are a group of genetic disorders associated with metabolic disorders in cells. These diseases are characterized by the accumulation of various substances that can lead to serious health consequences. In this article we will look at the main types of storage diseases, their symptoms and treatment.

The main symptom of storage disease is the accumulation of excess substances in all tissues of the body. The causes of these diseases may be

Storage diseases are a group of genetic diseases that lead to the accumulation of various substances in the tissues and organs of the body, which can cause various symptoms and complications. These diseases can be hereditary or acquired, and also manifest themselves in different age groups. In this article we will look at the most common storage diseases and their possible causes and symptoms.

Hereditary storage diseases