Horizontal Pendular Nystagmus and Ataxia Secondary to Severe Hypomagnesemia.


Journal

Tremor and other hyperkinetic movements (New York, N.Y.)
ISSN: 2160-8288
Titre abrégé: Tremor Other Hyperkinet Mov (N Y)
Pays: England
ID NLM: 101569493

Informations de publication

Date de publication:
2024
Historique:
received: 26 04 2024
accepted: 10 07 2024
medline: 29 7 2024
pubmed: 29 7 2024
entrez: 29 7 2024
Statut: epublish

Résumé

Severe hypomagnesemia is an increasingly recognized cause of acute and reversible cerebellar ataxia, often accompanied by cerebellar oculomotor signs such as jerky horizontal or downbeat nystagmus and very rarely ocular flutter. This video illustrates horizontal pendular nystagmus in a patient with acute onset cerebellar ataxia associated with severe hypomagnesemia. Acquired pendular nystagmus can be distinguished from macrosaccadic oscillations and ocular flutter in that the former is composed of two slow phases of equal velocity and the latter of two fast phases of saccadic type with or without intersaccadic interval, respectively. It is most commonly associated with demyelinating, toxic, metabolic, and genetic disorders, but has not been reported in association with severe hypomagnesemia.

Sections du résumé

Background UNASSIGNED
Severe hypomagnesemia is an increasingly recognized cause of acute and reversible cerebellar ataxia, often accompanied by cerebellar oculomotor signs such as jerky horizontal or downbeat nystagmus and very rarely ocular flutter.
Phenomenology Shown UNASSIGNED
This video illustrates horizontal pendular nystagmus in a patient with acute onset cerebellar ataxia associated with severe hypomagnesemia.
Educational value UNASSIGNED
Acquired pendular nystagmus can be distinguished from macrosaccadic oscillations and ocular flutter in that the former is composed of two slow phases of equal velocity and the latter of two fast phases of saccadic type with or without intersaccadic interval, respectively. It is most commonly associated with demyelinating, toxic, metabolic, and genetic disorders, but has not been reported in association with severe hypomagnesemia.

Identifiants

pubmed: 39070062
doi: 10.5334/tohm.910
pmc: PMC11277473
doi:

Types de publication

Case Reports Journal Article Video-Audio Media

Langues

eng

Sous-ensembles de citation

IM

Pagination

38

Informations de copyright

Copyright: © 2024 The Author(s).

Déclaration de conflit d'intérêts

The authors have no competing interests to declare.

Auteurs

Marcos Polanco (M)

Neurology Service, University Hospital Marqués de Valdecilla-IDIVAL, Santander, Spain.

María Rivera (M)

Neurology Service, University Hospital Marqués de Valdecilla-IDIVAL, Santander, Spain.

Leire Manrique (L)

Neurology Service, University Hospital Marqués de Valdecilla-IDIVAL, Santander, Spain.

Carmen Lage (C)

Neurology Service, University Hospital Marqués de Valdecilla-IDIVAL, Santander, Spain.

Jon Infante (J)

Neurology Service, University Hospital Marqués de Valdecilla-IDIVAL, Santander, Spain.
Universidad de Cantabria (UC), Spain.
Centro de Investigación Biomédica en Red Enfermedades Neurodegenerativas (CIBERNED), ISCIII, Spain.

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Classifications MeSH