Vanishing White Matter Disease Presenting as Acute Febrile Encephalopathy: Case Report

Abstract

A 3.5-year-old male child patient with mild developmental delay presented with history of acute onset fever, encephalopathy, and dyskinesia. The patient was investigated for common etiologies and was managed supportively. His neuroimaging was suggestive of vanishing white matter (VWM) disease which was confirmed by clinical exome sequencing. The child had an eventful hospital stay followed by near-total recovery after 4 weeks. The case attempts to sensitize readers about the current perspectives pertaining to VWM disease.

Keywords

vanishing white matter disease - acute febrile encephalopathy - VWM

Authors' Contributions

J.N.G.: Case management, literature review, initial draft manuscript preparation and approval of final manuscript.

S.K.P.: Interpretation of neuroimaging, literature review, and approval of final manuscript.

A.S.: Case management, literature review, and initial draft manuscript preparation.

S.K.P.: Clinician-in-charge, critical review of manuscript for important intellectual content, and final approval of the version to be published.

Publikationsverlauf

Eingereicht: 15. August 2019

Angenommen: 18. September 2019

Artikel online veröffentlicht:
07. Dezember 2021

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