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

From National Research Council Canada

DOIResolve DOI: https://doi.org/10.1016/j.pediatrneurol.2012.06.015
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Affiliation
  1. National Research Council of Canada. Medical Devices
FormatText, Article
Abstract
Krabbe 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
In
  • Pediatric Neurology 47, no. 4 (October 2012): 299–302.
LanguageEnglish
Peer reviewedYes
IdentifierS0887899412003104
NPARC number21268840
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Record identifiered355650-df13-4b9f-8684-4cbbc03977b2
Record created2013-11-14
Record modified2020-04-21
Date modified: