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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 ...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Thieme Revinter Publicações Ltda.
2021
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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. |
format | Online Article Text |
id | pubmed-8321649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Thieme Revinter Publicações Ltda. |
record_format | MEDLINE/PubMed |
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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