An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype

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Correspondence to Francesco Nicita.

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This case report study does not require ethical approval at our institution.

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Written informed consent was obtained by patient's parents for performing genetic analysis according to the Declaration of Helsinki. Parents gave their written consent for publishing the picture of the patient.

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Nicita, F., Graziola, F., Vigevano, F. et al. An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype. Acta Neurol Belg 119, 619–620 (2019). https://doi.org/10.1007/s13760-019-01087-6

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Keywords

  • Leukodystrophy
  • Demyelinating
  • GALC
  • Krabbe disease
  • Galactocerebrosidase
  • Neuropathy