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 syndr...
Found on
http://en.wikipedia.org/wiki/Flynn–Aird_syndrome
<syndrome> A familial syndrome characterised by muscle wasting, ataxia, dementia, skin atrophy, and ocular anomalies. ... (05 Mar 2000) ...
Found on
http://www.encyclo.co.uk/local/20973
(flin´ ārd´) a rare autosomal dominant syndrome with abnormalities of the nervous system and ectodermal structures, including cataracts, retinitis pigmentosa, myopia, dental caries, skin atrophy and ulceration, peripheral neuropathy, ataxia, deafness, and cystic bone changes.
Found on
http://www.encyclo.co.uk/local/21001
Type: Term Pronunciation: flin ārd Definitions: 1. a familial syndrome characterized by muscle wasting, ataxia, dementia, skin atrophy, dental caries, joint stiffness, retinitis pigmentosa, and progressive sensorineural hearing loss; autosomal dominant inheritance.
Found on
http://www.medilexicon.com/medicaldictionary.php?t=87988
No exact match found.
