Redera Syndrome

Roeder syndrome is a rare and poorly understood ophthalmological disease that manifests itself in connection with neurological disorders. This pathology leads to the fact that a person can become completely blind without surgical treatment. Roeder syndrome most often affects men, but the disease can also occur in women of all ages. It was first described in the 20th century by Norwegian ophthalmologist and neurologist Georg Roeder, who called it trigeminal syndrome.

Roeder's syndrome is a hereditary disease, but it has not been proven whether it is directly related to the development of a tumor of the base of the skull and the resulting compression of the triceps nerve. Symptoms of the disease include vision problems, flashes of light, and increased sensitivity to light. A person suffering from this syndrome may lose their vision if the condition is not treated, making it impossible for them to work normally. Treatment for the syndrome involves surgery to the brain or throat. A neurologist reconstructs the nerve endings that cause vision problems. Paratrigeminal syndrome is a disease of the central nervous system. It is characterized by an increase in symptoms of neurological problems that prevent a person from leading a full life. The main task in this case is to perform the operation and rehabilitation of the patient after surgery. In addition, the disease threatens a person with disability. The main symptoms of the pathology include: - compression of the spinal nerves due to a tumor - visual impairment - partial or complete blindness According to neurologists, at least two people suffer from paratrigeminal syndrome

Below is a description of Rader syndrome, also known as paratrigeminal syndrome, a rare autosomal dominant disorder caused by a mutation in the ATP2C1 gene. In this article I will tell you more about redder syndrome.

**Roeder syndrome** is a rare hereditary disease characterized by dysfunction of the trigeminal nerve, which leads to various symptoms. With this disease, patients may experience various symptoms, including facial pain, vision problems, and decreased sensitivity of the skin and mucous membranes. In particular, with reder syndrome, patients may experience discomfort in the eyes, ears and nose, as well as suffer from headaches, pain in the teeth, jaw and nose. Also, as the patients themselves note, with this condition, “many” digestive problems may occur. Despite,