Nystagmus Congenital Hereditary

Congenital hereditary nystagmus: causes, symptoms and treatment

Congenital hereditary nystagmus, also known as congenital hereditary nystagmus, is a rare genetic disorder that results in involuntary, rhythmic eye movements. This type of nystagmus can occur in children already in the first months of life and throughout life.

Causes:

Congenital hereditary nystagmus is caused by the presence of genetic mutations that are inherited from parents. These mutations can affect various genes related to the function of the eye and nervous system, resulting in poor coordination of eye movements.

Symptoms:

The main symptom of congenital hereditary nystagmus is involuntary eye movements, which can be horizontal, vertical or circular. These movements may intensify when the gaze is fixed on certain objects, fatigue or stress. Poor eye coordination can also cause difficulty seeing, especially in poor lighting conditions or when the eyes move rapidly.

Treatment:

Congenital hereditary nystagmus has no cure, but symptoms can be improved by various methods, including wearing special glasses, treating abnormalities of the visual cortex, exercises to improve eye coordination and other methods. In some cases, surgical correction may be recommended, although the effectiveness of this method may be limited.

In conclusion, congenital hereditary nystagmus is a rare genetic disorder that results in involuntary, rhythmic eye movements. Although there is no specific treatment, symptoms can be improved by various methods, which can significantly improve the patient's quality of life. If you suspect congenital hereditary nystagmus, consult your doctor for diagnosis and treatment.

Congenital hereditary nystagmus (CHN) is a condition in which the eyes constantly move from side to side and are unable to focus on one object. This is a serious disease that can lead to visual impairment and social adaptation in children and adults. The causes of VND are not yet known, but it is associated with genetic inheritance.

There are several forms of VNN, and each of them has its own characteristics. One of the most common forms is paralytic nystagmus, which is characterized by rapid movement of the eyeballs, but lack of focus. Another form is fixed nystagmus, with slow eye movement when trying to focus. Another form of VNN is oscillatory nystagmus with weak eye movement, which is observed in children with delayed speech development.

Treatment of VNN depends on its form and severity of the disease. In some cases, medication or physical therapy is sufficient, while other patients require surgery. Some people with SLI can learn to control their eye movements and improve their vision without surgery.

SUD may result from genetic disorders