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

doi:10.1016/j.neurol.2010.07.001

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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...

Topics

Aged
Anti-Inflammatory Agents
Brachial Plexus Neuritis
Dysphonia
Dyspnea
Humans
Immunosuppressive Agents
Male
Methylprednisolone
Mutation
Paralysis
Phrenic Nerve
Septins

Source

Open in PubMed

Identifiers

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

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