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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Vydané v:	Annals of medicine (Helsinki) Ročník 47; číslo 6; s. 506 - 511
Hlavní autori:	Nikoskinen, Tuuli, Schmidt, Eeva-Kaisa, Strbian, Daniel, Kiuru-Enari, Sari, Atula, Sari
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	England Taylor & Francis 18.08.2015
Predmet:	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
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