Hearing problems in patients with hereditary gelsolin amyloidosis

BACKGROUND: Gelsolin amyloidosis (AGel amyloidosis) is a hereditary form of systemic amyloidosis featuring ophthalmological, neurological and cutaneous symptoms. Previous studies based mainly on patients’ self-reporting have indicated that hearing impairment might also be related to the disease, con...

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Detalles Bibliográficos
Autores principales: Mustonen, Tuuli, Sivonen, Ville, Atula, Sari, Kiuru-Enari, Sari, Sinkkonen, Saku T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543933/
https://www.ncbi.nlm.nih.gov/pubmed/34689817
http://dx.doi.org/10.1186/s13023-021-02077-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8543933/
https://www.ncbi.nlm.nih.gov/pubmed/34689817
http://dx.doi.org/10.1186/s13023-021-02077-9

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