A case of familial amyloidotic polyneuropathy with a rare Phe33Leu mutation in the TTR gene
Journal
Journal of the Formosan Medical Association
Journal Volume
113
Journal Issue
8
Pages
575-576
Date Issued
2014
Author(s)
SDGs
Other Subjects
amyloid; prealbumin; adult; anhidrosis; areflexia; article; autonomic dysfunction; case report; clinical feature; conformational transition; diarrhea; dizziness; erectile dysfunction; familial amyloid polyneuropathy; gene; gene mutation; gene sequence; genetic counseling; genetic screening; human; hyperalgesia; limb weakness; male; middle aged; molecular mimicry; muscle atrophy; nerve conduction; orthostatic hypotension; polyneuropathy; rare disease; restrictive cardiomyopathy; TTR gene; unsteadiness; genetics; mutation; nucleotide sequence; pathology; DNA Mutational Analysis; Humans; Male; Middle Aged; Mutation; Polyneuropathies; Prealbumin
Publisher
Elsevier B.V.
Type
journal article