International Archives of Otorhinolaryngology (Jul 2024)
Peripheral Auditory Pathway and ABR Characterization in Adults with Williams Syndrome
Abstract
Introduction Williams syndrome (WS) is a genetic disorder caused by a microdeletion in chromosome 7, affecting ∼ 28 genes. Studies have demonstrated conductive losses seemingly related to the absence of the elastin gene and mild to profound sensorineural losses due to cochlear fragility.
Keywords