Hemiconvulsion–hemiplegia syndrome and primary human herpesvirus 7 infection

We report a case of hemiconvulsion–hemiplegia (HH) syndrome. An 18-month-old female infant had a hemiconvulsion followed by left hemiplegia. Magnetic resonance imaging immediately after the onset of hemiplegia showed high intensity in the right hemisphere in diffusion-weighted images (DWI), while T1...

Full description

Saved in:
Bibliographic Details
Published inBrain & development (Tokyo. 1979) Vol. 26; no. 6; pp. 412 - 414
Main Authors Kawada, Jun-ichi, Kimura, Hiroshi, Yoshikawa, Tetsushi, Ihira, Masaru, Okumura, Akihisa, Morishima, Tsuneo, Hayakawa, Fumio
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.09.2004
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:We report a case of hemiconvulsion–hemiplegia (HH) syndrome. An 18-month-old female infant had a hemiconvulsion followed by left hemiplegia. Magnetic resonance imaging immediately after the onset of hemiplegia showed high intensity in the right hemisphere in diffusion-weighted images (DWI), while T1- and T2-weighted images were normal. Single photon emission computed tomography showed hypoperfusion of the right hemisphere in the acute phase. Virological analyses proved primary human herpesvirus 7 (HHV-7) infection. DWI are useful for the early evaluation of HH syndrome. Vascular disorders due to HHV-7 infection may have been related to the development of HH syndrome in this patient.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:0387-7604
1872-7131
DOI:10.1016/j.braindev.2003.12.003