Prolonged survival and serial magnetic resonance imaging/magnetic resonance spectroscopy changes in infantile Krabbe disease

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DOIResolve DOI: http://doi.org/10.1016/j.pediatrneurol.2012.06.015
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TypeArticle
Journal titlePediatric Neurology
ISSN08878994
Volume47
Issue4
Pages299302
AbstractKrabbe disease may present during infancy, late infancy, or adulthood. Earlier-onset disease is associated with shorter survival times. We present a case of infantile onset Krabbe disease with prolonged survival, initial intracranial optic nerves and optic chiasm hypertrophy, and serial changes on cranial magnetic resonance imaging and magnetic resonance spectroscopy.
Publication date
LanguageEnglish
AffiliationMedical Devices; National Research Council Canada
Peer reviewedYes
IdentifierS0887899412003104
NPARC number21268840
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Record identifiered355650-df13-4b9f-8684-4cbbc03977b2
Record created2013-11-14
Record modified2016-05-09
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