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Forschungsdatenbank PMU-SQQUID

Mitochondrial Disease and Hearing Loss in Children: A Systematic Review.
Roesch, S; OSullivan, A; Zimmermann, G; Mair, A; Lipuš, C; Mayr, JA; Wortmann, SB; Rasp, G;
Laryngoscope. 2022; 132(12):2459-2472
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PMU-Autor/inn/en

Mair Alois
Mayr Johannes A.
O'Sullivan Anna
Rasp Gerd
Rösch Sebastian
Wortmann Saskia
Zimmermann Georg Johannes

Abstract

Hearing loss is a clinical symptom, frequently mentioned in the context of mitochondrial disease. With no cure available for mitochondrial disease, supportive treatment of clinical symptoms like hearing loss is of the utmost importance. The aim of this study was to summarize current knowledge on hearing loss in genetically proven mitochondrial disease in children and deduce possible and necessary consequences in patient care.


Useful keywords (using NLM MeSH Indexing)

Humans

Systematic Reviews as Topic

Hearing Loss*/diagnosis

Deafness*

Hearing Loss, Sensorineural*

Mitochondrial Diseases*/complications


Find related publications in this database (Keywords)

mitochondrial disease
mitochondriopathy
mitochondria
hearing
hearing loss
audiometry
audiometric testing
auditory neuropathy
brainstem evoked auditory potentials
treatment