Leber's hereditary optic neuropathy (LHON) - loss of central vision

Leber’s hereditary optic neuropathy is the phenomenon of degeneration of the rentinal ganglion cells and their axons which as a result leads to a loss of central vision of the human eyesight.

This syndrome of Leber’s hereditary optic neuropathy generally affects not the older people but the younger people in a society.

Leber’s hereditary optic neuropathy generally takes place to do some dna mutations that takes place in the human eye. More information about the Leber’s hereditary optic neuropathy syndrome should be acquired from an expert human eyes specialist that can guide the patients of Leber’s hereditary optic neuropathy with more strategic information on the Leber’s hereditary optic neuropathy syndrome.