Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An under‐recognized condition

Mostrar otras versiones (1)

We report the case of a teenager with neurofibromatosis type 2 (NF2) presenting a locked‐in syndrome due to a brainstem ischemic syndrome. The presence of sudden or rapidly worsening onset of neurological deficits in NF2 patients should evoke this underknown entity and not only tumors as predisposed...

Descripción completa

Detalles Bibliográficos
Autores principales: Blauen, Aglaë, Lenfant, Christine, Duprez, Thierry, Nassogne, Marie‐Cécile
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Erratum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811064/
https://www.ncbi.nlm.nih.gov/pubmed/36619483
http://dx.doi.org/10.1002/ccr3.6804
_version_ 1784863449669435392
author Blauen, Aglaë
Lenfant, Christine
Duprez, Thierry
Nassogne, Marie‐Cécile
author_facet Blauen, Aglaë
Lenfant, Christine
Duprez, Thierry
Nassogne, Marie‐Cécile
author_sort Blauen, Aglaë
collection PubMed
description We report the case of a teenager with neurofibromatosis type 2 (NF2) presenting a locked‐in syndrome due to a brainstem ischemic syndrome. The presence of sudden or rapidly worsening onset of neurological deficits in NF2 patients should evoke this underknown entity and not only tumors as predisposed by NF2.
format Online
Article
Text
id pubmed-9811064
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-98110642023-01-05 Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An under‐recognized condition Blauen, Aglaë Lenfant, Christine Duprez, Thierry Nassogne, Marie‐Cécile Clin Case Rep Erratum We report the case of a teenager with neurofibromatosis type 2 (NF2) presenting a locked‐in syndrome due to a brainstem ischemic syndrome. The presence of sudden or rapidly worsening onset of neurological deficits in NF2 patients should evoke this underknown entity and not only tumors as predisposed by NF2. John Wiley and Sons Inc. 2023-01-03 /pmc/articles/PMC9811064/ /pubmed/36619483 http://dx.doi.org/10.1002/ccr3.6804 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Erratum
Blauen, Aglaë
Lenfant, Christine
Duprez, Thierry
Nassogne, Marie‐Cécile
Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An under‐recognized condition
title Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An under‐recognized condition
title_full Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An under‐recognized condition
title_fullStr Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An under‐recognized condition
title_full_unstemmed Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An under‐recognized condition
title_short Subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: An under‐recognized condition
title_sort subacute brainstem ischemic syndrome in juvenile neurofibromatosis type 2: an under‐recognized condition
topic Erratum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811064/
https://www.ncbi.nlm.nih.gov/pubmed/36619483
http://dx.doi.org/10.1002/ccr3.6804
work_keys_str_mv AT blauenaglae subacutebrainstemischemicsyndromeinjuvenileneurofibromatosistype2anunderrecognizedcondition
AT lenfantchristine subacutebrainstemischemicsyndromeinjuvenileneurofibromatosistype2anunderrecognizedcondition
AT duprezthierry subacutebrainstemischemicsyndromeinjuvenileneurofibromatosistype2anunderrecognizedcondition
AT nassognemariececile subacutebrainstemischemicsyndromeinjuvenileneurofibromatosistype2anunderrecognizedcondition

Ejemplares similares