What Is the Role of Sensorineural Hearing Loss in Fabry Disease Screening?

OBJECTIVE: Fabry disease is a rare hereditary lysosomal storage disease caused by the deficiency of alpha-galactosidase A (α-GLA). Although sensorineural hearing loss is common in Fabry disease, there are no studies in the literature that have screened a population with sensorineural hearing loss fo...

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Detalles Bibliográficos
Autores principales: Köroğlu, Ekin Yiğit, Gökçay Canpolat, Asena, Yılmaz, Suna, Demir, Özgür
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2023
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506525/
https://www.ncbi.nlm.nih.gov/pubmed/37727814
http://dx.doi.org/10.4274/tao.2023.2023-3-10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10506525/
https://www.ncbi.nlm.nih.gov/pubmed/37727814
http://dx.doi.org/10.4274/tao.2023.2023-3-10

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