Dysplasia Encephalo-ophthalmic Familial

Familial encephalo-ophthalmic dysplasia (FED) is a rare inherited disease characterized by abnormal development of the brain and eyes. It can come in different forms and can be mild or severe.

Symptoms of DES may include:

– Developmental delay - children with DES may lag behind their peers in development
– Vision problems - such as squint, myopia, farsightedness, etc.
– Impaired coordination of movements - for example, difficulty walking and running
– Mental retardation – some people with DES may have mental retardation

Diagnosis of DES is carried out using genetic testing and other research methods. Treatment may include surgery, medication, and rehabilitation.

However, although DES is a rare disease, it can have serious consequences on a person's life. Therefore, if you suspect DES, you need to consult a specialist for diagnosis and treatment.