婴儿型克拉伯病的长期生存和磁共振成像/磁共振波谱学的系列变化。
Prolonged survival and serial magnetic resonance imaging/magnetic resonance spectroscopy changes in infantile Krabbe disease.
机构信息
Section of Neurology, Faculty of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.
出版信息
Pediatr Neurol. 2012 Oct;47(4):299-302. doi: 10.1016/j.pediatrneurol.2012.06.015.
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.
摘要
克拉伯病可在婴儿期、晚婴儿期或成年期发病。发病较早的患者存活时间更短。我们报告了一例婴儿期发病的克拉伯病，患者存活时间延长，最初颅内视神经和视交叉肥大，并在头颅磁共振成像和磁共振波谱上连续变化。
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