Teaching NeuroImages: Slowly progressive hypertrophic brachial plexopathy due to SEPT9 mutation

Neurology. 2020 Jul 7;95(1):e109-e110. doi: 10.1212/WNL.0000000000009739. Epub 2020 Jun 10.

Authors

Paulo Victor Sgobbi de Souza¹, Eduardo Augusto Gonçalves¹, Bruno de Mattos Lombardi Badia¹, Igor Braga Farias¹, Luiz Henrique Libardi Silva¹, Mario Teruo Yanagiura¹, Wladimir Bocca Vieira de Rezende Pinto², Acary Souza Bulle Oliveira¹

Affiliations

¹ From the Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), Brazil.
² From the Division of Neuromuscular Diseases, Department of Neurology and Neurosurgery, Federal University of São Paulo (UNIFESP), Brazil. [email protected].

PMID: 32522797
DOI: 10.1212/WNL.0000000000009739

No abstract available

Publication types

Case Reports

MeSH terms

Brachial Plexus Neuropathies / genetics*
Genetic Predisposition to Disease / genetics*
Humans
Male
Middle Aged
Mutation
Septins / genetics*

Substances

SEPTIN9 protein, human
Septins