Episode 3035
Flynn–Aird syndrome
Mon, 2025-Aug-25 00:09 UTC
Length - 2:20
Direct Link
Welcome to random Wiki of the Day, your journey through Wikipedia's vast and varied content, one random article at a time.
The random article for Monday, 25 August 2025, is Flynn–Aird syndrome.
Flynn–Aird syndrome is a rare, hereditary, neurological disease that is inherited in an autosomal dominant fashion. The syndrome involves defects in the nervous, auditory, skeletal, visual, and endocrine systems and encompasses numerous symptoms, bearing striking similarity to other known syndromes of neuroectodermal nature such as: Werner syndrome, Cockayne syndrome and Refsum syndrome.
The onset of Flynn–Aird syndrome typically occurs between ten and twenty years of age, however, the earliest case was diagnosed at age seven. As the syndrome progresses, initial symptoms tend to intensify and new symptoms become apparent. Unlike related syndromes and despite the intensity of symptoms in the disease progression, Flynn–Aird syndrome does not appear to shorten life expectancy.
The disease is characterized by early-onset dementia, ataxia, muscle wasting, skin atrophy, and eye abnormalities. In addition, patients have the potential of developing a number of other related symptoms such as: cataracts, retinitis pigmentosa, myopia (nearsightedness), dental caries, peripheral neuropathy (peripheral nerve damage), deafness, and cystic bone changes. This syndrome was first discovered in the early 1950s by American neurologists P. Flynn and Robert B. Aird who analyzed one family lineage inheritance pattern of this disease.
This recording reflects the Wikipedia text as of 00:09 UTC on Monday, 25 August 2025.
For the full current version of the article, see Flynn–Aird syndrome on Wikipedia.
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Until next time, I'm neural Salli.
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