Congenital Amaurosis

Below you will find more information about Congenital Amaurosis from Medigest. If you believe that you are suffering from any of the symptoms of Congenital Amaurosis it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Congenital Amaurosis and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Congenital Amaurosis comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Congenital amaurosis is another name for Leber's hereditary optic neuropathy (LHON). It is a degenerative eye disease characterized by the inflammation of the retinal ganglion cells. This condition may lead to permanent loss of vision.


Diagnostic tests like optical coherence topography and other eye examinations are conducted to determine the presence inflamed nerves in the anterior area.


Anti-inflammatory drugs are used to treat the disease.

Symptoms and Signs

The first symptoms of the disease include reduced or blurry vision. After a few weeks, edema-liked clusters fibers will start to develop in the eye, taking over the retina and causing pain and irritation.


This disease is a result of a genetic mutation of the cells' mitochondria.

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