Eclina Disease

Introduction

Ecline disease is a genetic disorder that causes problems with the development of the brain and nervous system in newborns. This is a rare disease that is rarely heard of in everyday life. In this article we will look at the causes and symptoms of eclin disease, as well as modern methods of diagnosis and treatment.

Causes of eclin disease

Ecclina disease is caused by a gene disorder on chromosome 22. This disorder is one of many genetic disorders associated with the development of the nervous system. Ecclin disease can be caused by a mutation in the genes responsible for the synthesis of proteins necessary for the normal formation of nerve cells and fibers. Another cause of eclinova may be intoxication with amniotic fluid in the early stages of pregnancy.

Symptoms of eclinova

One of the most common symptoms of eclinova is developmental delay in the fetus, which can manifest itself in different forms. Typically, delays in motor development occur due to impaired motor coordination. The baby may have slow growth of the head, limbs, and trunk, or may be born with a small head size. Less commonly, symptoms may appear before the mother is born. These include protein-carbohydrate edema or diabetes, increased levels of proteins in the blood plasma.

Diagnosis of eclinova

Traditional method