Spongioblastosis

Spongiobastosis is a genetic disease consisting of an increase in the number of nervous tissue cells (spongioblasts). In this article we will look at the causes, signs and treatment of blastosis spongiosum.

Causes of spongioblastosis:

Spongioiblastosis can be caused by various reasons, but it is not yet known exactly what is the main trigger for the development of the disease. Among the main causes are the following factors: - mutations in the ASXL1 or ASXL2 genes - the presence of mutations in other genes responsible for the functioning of the nervous system, for example, in the RB1 gene - radiation exposure

Signs of spongioblastosis

The most common manifestation of spongiform blastosis is developmental delay. Children with this disease often look younger than their age, they are unable to stay in a sitting position on their own, often fall, and are afraid of the world around them. With spongioblastosis, there may also be mental disorders, so the child may be in a state of fear or in manic delight. Spongy children often experience disruption of the functioning of organs and body systems, such as gastrointestinal insufficiency, decreased immunity, and pituitary hyperplasia. One of the most dangerous forms of spongy disease can be convulsive syndrome. Such children experience a high temperature, a deterioration in their general condition, followed by loss of consciousness, convulsions and vomiting, leading to an imbalance in the water balance in the body. During this period, the child must be provided with qualified assistance. Frequent fainting in a child may also be a sign of the disease. In addition, this condition is characterized by cases of severe irritability that arise against the background