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Article

[Familial amyloid neuropathies].

Revue neurologique - 1 Jan 1993

Julien J

Abstract excerpt

Recent advances in molecular biology have given improved knowledge of familial amyloidotic polyneuropathies (FAP). FAP, originally described in Portuguese patients have been observed in many countries. These neuropathies are characterized by a sensory motor deficit beginning in the lower limbs and associated with autonomic nervous system involvement and tropic lesions of the feet in a few patients. FAP are...

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Identifiers

PMID: 8023063

Genes

FAP
TTR

Provenance

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

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