Case Report: Parsonage-Turner syndrome due to SEPTIN9 mutation: report of an Italian family with childhood onset and review of the literature

Case Report: Parsonage-Turner syndrome due to SEPTIN9 mutation: report of an Italian family with childhood onset and review of the literature

AimParsonage-Turner syndrome, also known as neuralgic amyotrophy affects the brachial plexus and includes idiopathic (INA) and rare hereditary forms (HNA). Mutations in the SEPTIN9 gene, which encodes a cytoskeletal GTPase, have been implicated in HNA. While Parsonage-Turner syndrome is typically ad...

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Bibliographic Details
Main Authors: Luca Bosisio, Matteo Cataldi, Marina Grandis, Barbara Tappino, Monica Traverso, Francesco Germano, Lino Nobili, Chiara Fiorillo
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-08-01
Series:Frontiers in Pediatrics
Subjects:
Parsonage-Turner syndrome
SEPTIN9
children neuropathy
HNA
mutation
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2025.1589397/full
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