Hearing problems in patients with hereditary gelsolin amyloidosis

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 h...

Source: Orphanet Journal of Rare Diseases - October 24, 2021 Category: Internal Medicine Authors: Tuuli Mustonen, Ville Sivonen, Sari Atula, Sari Kiuru-Enari and Saku T. Sinkkonen Tags: Research Source Type: research