Subtle neuropsychiatric and neurocognitive changes in hereditary gelsolin amyloidosis (AGel amyloidosis)

Hereditary gelsolin amyloidosis (AGel amyloidosis) is an autosomal dominant form of systemic amyloidosis caused by a c.640G>A or c.640G>T mutation in the gene coding for gelsolin. Principal clinical manifestations include corneal lattice dystrophy, cranial neuropathy and cutis laxa with vascul...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Autori principali: Mari Kantanen, Sari Kiuru-Enari, Oili Salonen, Markku Kaipainen, Laura Hokkanen
Natura: Artigo
Lingua:Inglês
Pubblicazione: PeerJ Inc. 2014-07-01
Serie:PeerJ
Soggetti:
Hereditary amyloidosis
Gelsolin amyloidosis
Neuropsychological testing
Visuoconstructional problems
Depression
Magnetic resonance imaging
Accesso online:https://peerj.com/articles/493.pdf
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi