Leber Hereditary Optic Neuropathy is a rare, mitochondrially-inherited condition that causes sudden, painless central vision loss. It primarily affects young men, though it can occur at any age and in any gender. Because it is passed down through mitochondrial DNA, it typically affects one eye first, with the second eye following within weeks to months. Research into LHON has expanded significantly, focusing on how to work around the inherited mitochondrial defect to support visual function.

Associate Professor, Vitreo-Retina Surgeon. 10+ Years Experience

Senior Consultant Ophthalmologist & Eye Surgeon· 26+ yrs experience

Consultant Ophthalmologist & Eye Surgeon, MD, DO .16+ Years Experience

I am very satisfied with the services at Stem Cell Cure. The team is very professional and knowledgeable. They provided good guidance and ensured every step of the process was smooth and comfortable

Stem Cell Cure India made me believe in the treatment right from the first consultation. The doctors went through the therapy in depth and the staff was always there to help. I was secure and respected during my procedure
“Not currently. There is no treatment that corrects the underlying mitochondrial mutation. Care focuses on supporting remaining visual function and monitoring for any spontaneous recovery, which occurs in a minority of cases.”
“Genetic counselling is recommended for at-risk maternal relatives, as this helps with early monitoring and informed family planning decisions.”
“Suitability depends on how much viable optic nerve tissue remains and the stage of disease; our team reviews genetic and OCT/visual field results before advising on realistic expectations.”

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