Progressive external ophthalmoplegia - what does this mean
Progressive external ophthalmoplegia is a rare genetic disorder caused by mutations in mitochondrial dna, resulting in a decrease in the function of the muscles that control eye movement. symptoms usually begin in the teenage years and include droopy eyelids, double vision, and difficulty moving the eyes in all directions. over time, the condition can lead to complete paralysis of the eye muscles, resulting in a complete inability to move the eyes.
What happens during the disease - progressive external ophthalmoplegia
Progressive external ophthalmoplegia (peo) is a rare disorder caused by mutations in the mitochondrial dna, leading to an impaired ability of the mitochondria to produce energy. this results in a decrease in the amount of atp available for the muscles of the eye, leading to progressive weakness of the muscles surrounding the eye, and resulting in difficulty in moving the eye.
Treatment and Medical Assistance
Main Goal: To reduce the symptoms of Progressive External Ophthalmoplegia
- Regular physical exercise and stretching
- Regular eye exercises
- Medications to reduce muscle weakness
- Intravenous immunoglobulin (IVIG) therapy
- Plasmapheresis
- Surgery to repair muscle damage
- Vitamin E supplementation
- Coenzyme Q10 supplementation
- Speech therapy
- Occupational therapy
- Nutritional counseling
8 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Progressive external ophthalmoplegia - Prevention
Progressive external ophthalmoplegia can be prevented by early diagnosis and treatment of underlying causes, such as mitochondrial diseases, hormone deficiencies, or thyroid problems. it is also important to maintain a healthy lifestyle and diet rich in antioxidants, as well as avoiding excessive exposure to ultraviolet radiation.