Infantile hereditary optic atrophy is otherwise known as Behr syndrome. This condition begins early childhood, with ataxia, mental retardation, pes cavus, urinary incontinence, and pyramidal tract signs. This is caused due to the mutation in the OPA1 (OPA1 mitochondrial dynamin-like GTPase) genes.
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Kindly explain about infantile hereditary optic atrophy.
Query: Hello doctor, My wife was diagnosed with infantile hereditary optic atrophy when she was young. She is now 52. Can you provide me with some up-to-date information or a webpage that explains the disease, its symptoms, if it goes by any other name or is a symptom of another disease, etc? I can only f... Read Full »
Answer: Hello, Welcome to icliniq.com. I am very sorry about your wife, optic atrophy is an irreversible process and once the optic nerve has atrophied, there is nothing we can do. It is regarded as the end stage of the inflammatory process of the optic nerve called optic neuritis, optic neuropathy. Regar... Read Full »