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Article

[Severe form of hereditary neuralgic amyotrophy without SEPT9 gene mutation].

Revue neurologique - 1 Feb 2011

Cosson A, Mathieu A, Sevrin P, Nollet S, Tatu L

Abstract excerpt

INTRODUCTION: Hereditary neuralgic amyotrophy (HNA) is a rare condition characterized by recurrent episodes of painful paralysis preferentially affecting the brachial plexus. It is often linked to a mutation in the SEPT9 gene. CASE REPORT: A 69-year-old female patient experienced a dozen episodes of severe neurological deficit mainly affecting the brachial plexus and the phrenic and recurrent nerves. The...

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PMID: 20800251
DOI: 10.1016/j.neurol.2010.07.001

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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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