Natural course of Finnish gelsolin amyloidosis

Background. Finnish type of hereditary gelsolin amyloidosis (FGA) is one of the most common diseases of Finnish disease heritage. Existing FGA knowledge is based only on smaller patient series, so our aim was to elucidate the natural course of the disease in a comprehensive sample of patients and to...

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Veröffentlicht in:	Annals of medicine (Helsinki) Jg. 47; H. 6; S. 506 - 511
Hauptverfasser:	Nikoskinen, Tuuli, Schmidt, Eeva-Kaisa, Strbian, Daniel, Kiuru-Enari, Sari, Atula, Sari
Format:	Journal Article
Sprache:	Englisch
Veröffentlicht:	England Taylor & Francis 18.08.2015
Schlagworte:	Adult Aged Aged, 80 and over Amyloidosis Amyloidosis - epidemiology Amyloidosis - genetics Amyloidosis - metabolism Amyloidosis - pathology Amyloidosis, Familial - epidemiology Amyloidosis, Familial - genetics Amyloidosis, Familial - metabolism Amyloidosis, Familial - pathology Corneal Dystrophies, Hereditary - epidemiology Corneal Dystrophies, Hereditary - genetics Corneal Dystrophies, Hereditary - metabolism Corneal Dystrophies, Hereditary - pathology course Disease Progression familial Female Finland - epidemiology Finnish type amyloidosis Gelsolin - genetics Gelsolin - metabolism gelsolin-related amyloidosis Humans Male Meretoja syndrome Middle Aged Mutation Registries Finland familial gelsolin-related amyloidosis course Amyloidosis disease progression Meretoja syndrome Finnish type amyloidosis
ISSN:	0785-3890, 1365-2060, 1365-2060
Online-Zugang:	Volltext
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