Código QR (código de barras bidimensional)

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...

ver descrição completa

Na minha lista:
Principais autores: Luca Bosisio, Matteo Cataldi, Marina Grandis, Barbara Tappino, Monica Traverso, Francesco Germano, Lino Nobili, Chiara Fiorillo
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2025-08-01
coleção:Frontiers in Pediatrics
Assuntos:
Parsonage-Turner syndrome
SEPTIN9
children neuropathy
HNA
mutation
Acesso em linha:https://www.frontiersin.org/articles/10.3389/fped.2025.1589397/full
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registros relacionados