Clouston's palsy

Clousstone's palsy is a neurodevelopmental complication that can cause loss of sensation and motor function in the arms and legs. This condition is quite rare and affects children between the ages of one and six years.

Symptoms of Clouston's palsy.

Signs of this disease can appear either simultaneously or separately, depending on the nature of the changes as the disease progresses. Most cases are diagnosed in the second year of life before the age of 3 years.

The main cause of paralysis is the development of motor or sensory neuropathy (the inability of muscles to feel or move), which is caused by a hereditary predisposition. In most cases, the disease is caused by dysfunction of anti-dietary molecules that control the development of nervous tissue. Due to DNA damage, these molecules begin to negatively affect neurons and surrounding tissues. The *first symptom* is the child's lethargy, but after a few months his condition noticeably worsens. The child stops moving and recognizing his family, and his muscles gradually atrophy. Paralysis occurs due to an imbalance of protein molecules, which makes nerve cells more susceptible to aging. This makes delivery more difficult.