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Hearing Loss in Mucopolysaccharidosis

Introduction  Mucopolysaccharidosis (MPS) is a set of rare diseases caused by deficiency of lysosomal enzymes that lead to the accumulation of glycosaminoglycans (GAG) in tissues and organs, which, in turn, is responsible for the multisystemic clinical, chronic, and progressive symptoms. Objective  ...

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Autores principales: Bicalho, Cibele Gomes, de Araújo Leão, Emília Katiane Embiruçu, de Andrade, Álvaro Muiños, Acosta, Angelina Xavier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Thieme Revinter Publicações Ltda. 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321649/
https://www.ncbi.nlm.nih.gov/pubmed/34377173
http://dx.doi.org/10.1055/s-0040-1712107
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author Bicalho, Cibele Gomes
de Araújo Leão, Emília Katiane Embiruçu
de Andrade, Álvaro Muiños
Acosta, Angelina Xavier
author_facet Bicalho, Cibele Gomes
de Araújo Leão, Emília Katiane Embiruçu
de Andrade, Álvaro Muiños
Acosta, Angelina Xavier
author_sort Bicalho, Cibele Gomes
collection PubMed
description Introduction  Mucopolysaccharidosis (MPS) is a set of rare diseases caused by deficiency of lysosomal enzymes that lead to the accumulation of glycosaminoglycans (GAG) in tissues and organs, which, in turn, is responsible for the multisystemic clinical, chronic, and progressive symptoms. Objective  To describe the profile of the otorhinolaryngological clinical examination and audiology tests of patients with MPS disease. Methods  The present study is a case series. The evaluation was performed, initially, in 24 patients with MPS types I, II, IIIA, IV and VI. Results  The most common hearing complaint was hearing loss, which was confirmed by audiology tests in almost 100% of the patients, most of whom presented conductive hearing loss. Conclusions  It is important to evaluate the complaints, physical examination, and audiology tests in patients with MPS. The otorhinolaryngologistshould be part of the group of professionals that follows these patients to better monitor their hearing and provide early hearing rehabilitation.
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spelling pubmed-83216492021-08-09 Hearing Loss in Mucopolysaccharidosis Bicalho, Cibele Gomes de Araújo Leão, Emília Katiane Embiruçu de Andrade, Álvaro Muiños Acosta, Angelina Xavier Int Arch Otorhinolaryngol Introduction  Mucopolysaccharidosis (MPS) is a set of rare diseases caused by deficiency of lysosomal enzymes that lead to the accumulation of glycosaminoglycans (GAG) in tissues and organs, which, in turn, is responsible for the multisystemic clinical, chronic, and progressive symptoms. Objective  To describe the profile of the otorhinolaryngological clinical examination and audiology tests of patients with MPS disease. Methods  The present study is a case series. The evaluation was performed, initially, in 24 patients with MPS types I, II, IIIA, IV and VI. Results  The most common hearing complaint was hearing loss, which was confirmed by audiology tests in almost 100% of the patients, most of whom presented conductive hearing loss. Conclusions  It is important to evaluate the complaints, physical examination, and audiology tests in patients with MPS. The otorhinolaryngologistshould be part of the group of professionals that follows these patients to better monitor their hearing and provide early hearing rehabilitation. Thieme Revinter Publicações Ltda. 2021-07 2020-09-24 /pmc/articles/PMC8321649/ /pubmed/34377173 http://dx.doi.org/10.1055/s-0040-1712107 Text en Fundação Otorrinolaringologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. ( https://creativecommons.org/licenses/by-nc-nd/4.0/ ) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License, which permits unrestricted reproduction and distribution, for non-commercial purposes only; and use and reproduction, but not distribution, of adapted material for non-commercial purposes only, provided the original work is properly cited.
spellingShingle Bicalho, Cibele Gomes
de Araújo Leão, Emília Katiane Embiruçu
de Andrade, Álvaro Muiños
Acosta, Angelina Xavier
Hearing Loss in Mucopolysaccharidosis
title Hearing Loss in Mucopolysaccharidosis
title_full Hearing Loss in Mucopolysaccharidosis
title_fullStr Hearing Loss in Mucopolysaccharidosis
title_full_unstemmed Hearing Loss in Mucopolysaccharidosis
title_short Hearing Loss in Mucopolysaccharidosis
title_sort hearing loss in mucopolysaccharidosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321649/
https://www.ncbi.nlm.nih.gov/pubmed/34377173
http://dx.doi.org/10.1055/s-0040-1712107
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