Flynn Aird syndrome
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
Flynn-Aird Syndrome is a rare, autosomal dominant, hereditary degenerative neurological disorder characterized by early-onset dementia, ataxia, muscle wasting, skin atrophy, and eye abnormalities. It may cause cataracts, retinitis pigmentosa, myopia, dental caries, peripheral neuropathy, deafness, and cystic bone changes. It was first identified in the 1950s by American neurologists P. Flynn and Robert B. Aird.
