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Updated: Apr 15, 2026

Neuro-rehabilitation Approach for Sudden Sensorineural Hearing Loss
Published on: January 25, 2016
Allan-Herndon-Dudley syndrome with unusual profound sensorineural hearing loss
Lucia Gagliardi1,2,3, Nathalie Nataren2,4, Jinghua Feng4,5
1Endocrine and Metabolic Unit, Royal Adelaide Hospital, North Terrace, Adelaide, Australia.
Abstract:
The Allan-Herndon-Dudley syndrome is caused by mutations in the thyroid hormone transporter, Monocarboxylate transporter 8 (MCT8). It is characterized by profound intellectual disability and abnormal thyroid function. We report on a patient with Allan-Herndon-Dudley syndrome (AHDS) with profound sensorineural hearing loss which is not usually a feature of AHDS and which may have been due to a coexisting nonsense mutation in Microphthalmia-associated transcription factor (MITF).
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