International Archives of Otorhinolaryngology (Jul 2024)

Peripheral Auditory Pathway and ABR Characterization in Adults with Williams Syndrome

  • Jacqueline Aquino do Nascimento,
  • Liliane Aparecida Fagundes Silva,
  • Alessandra Gianella Samelli,
  • Carla Gentile Matas

DOI
https://doi.org/10.1055/s-0044-1785457
Journal volume & issue
Vol. 28, no. 03
pp. e502 – e508

Abstract

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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.

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