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Article

[Familial amyloidosis, Finnish type with marked anhidrosis].

Rinsho shinkeigaku = Clinical neurology - 1 Mar 1996

Ishiguchi H, Shimoya K, Ohnishi A, Murai Y, Nakazato M, Hoshii Y

Abstract excerpt

Familial amyloidosis, Finnish type (FAF), is a gelsolin-related systemic amyloidosis that has an autosomal-dominant inheritance pattern and is clinically characterized by progressive cranial neuropathy, corneal lattice dystrophy and skin changes such as cutis laxa, blepharochalasis, and lichen amyloidosis. A 70-year-old Japanese male proband, who was believed to be originally from Fukuoka Prefecture, showed signs...

Read the complete abstract on PubMed

Topics

Aged
Amyloidosis
Female
Gelsolin
Humans
Hypohidrosis
Male
Middle Aged

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Mutation

Pedigree

Sweat Glands

Source

Identifiers

PMID: 8741346

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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