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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...
Autores principales: | Mustonen, Tuuli, Sivonen, Ville, Atula, Sari, Kiuru-Enari, Sari, Sinkkonen, Saku T. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
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 |
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