Article
The audiovestibular profile of Brown-Vialetto-Van Laere syndrome.
The Journal of laryngology and otology - 1 Nov 2021
Omar R, Rajput K, Sirimanna T, Rajput S, Pagarkar W
Abstract excerpt
BACKGROUND: Brown-Vialetto-Van Laere syndrome, a rare disorder associated with motor, sensory and cranial nerve neuropathy, is caused by mutations in riboflavin transporter genes SLC52A2 and SLC52A3. Hearing loss is a characteristic feature of Brown-Vialetto-Van Laere syndrome and has been shown in recent studies to be characterised by auditory neuropathy spectrum disorder. METHOD: This study reports the detailed...
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