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Título: Hearing loss in acromegaly : a review
Autor(es): Teixeira, Liane Sousa
Silva, Isabelle Braz de Oliveira
Sampaio, Andre Luiz Lopes
Oliveira, Carlos Augusto Pires de
Bahamad Júnior, Fayez
Assunto: Surdez
Acromegalia
Data de publicação: 2018
Editora: Fundação Otorrinolaringologia
Referência: TEIXEIRA, Liane Sousa et al. Hearing loss in acromegaly: a review. International Archives of Otorhinolaryngology, São Paulo, v. 22, n. 3, p. 313-316, jul. 2018. DOI: http://dx.doi.org/10.1055/s-0037-1603619. Disponível em: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1809-48642018000300313&lng=en&nrm=iso. Acesso em: 25 jan. 2019.
Abstract: Introduction Acromegaly is a chronic disease caused by growth hormone (GH) excess due to a GH-secreting pituitary adenoma in most cases. There is reasonable data to presume the possible influence of chronic GH and insulin-like growth factor I (IGF-I) hyperproduction on the anatomical structures involved in normal sound perception, and on its conductive and/or sensorineural part. Objectives To review the literature about acromegaly and hearing loss. Data Synthesis A systematic literature search was performed using the MEDLINE database, including hand-searching reference lists from original articles. The search was performed using the terms hearing loss and acromegaly, and only 5 studies were found. Conclusion The results are not consistent, but led to different conclusions. Therefore, more studies with greater numbers of patients with acromegaly are needed.
Unidade Acadêmica: Faculdade de Medicina (FMD)
Licença: International Archives of Otorhinolaryngology - This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY NC ND). Fonte: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1809-48642018000300313&lng=en&nrm=iso. Acesso em: 25 jan. 2019.
DOI: http://dx.doi.org/10.1055/s-0037-1603619
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