Palatal myoclonus in Krabbe disease

Brain Dev. 1991 Sep;13(5):355-8. doi: 10.1016/s0387-7604(12)80133-1.

Abstract

A seven-year-old girl with Krabbe disease presenting palatal myoclonus only when awake is reported. The patient was diagnosed as having Krabbe disease enzymatically at the age of eleven months. She developed rhythmical contractions of the soft palate, pharynx, larynx, lips and tongue at two years. The surface electromyography showed rhythmical 2 Hz electrical activities. The MRI disclosed markedly attenuated intensity in the midbrain, pons and medulla oblongata on T2-weighted images. Palatal myoclonus was not controlled by carbamazepine in therapeutic doses, but disappeared when the patient was asleep. This is the first reported case of Krabbe disease with palatal myoclonus.

Publication types

  • Case Reports

MeSH terms

  • Brain / pathology
  • Electrodiagnosis
  • Female
  • Humans
  • Infant
  • Leukodystrophy, Globoid Cell / complications*
  • Magnetic Resonance Imaging
  • Myoclonus / diagnosis
  • Myoclonus / etiology*
  • Myoclonus / physiopathology
  • Palatal Muscles* / physiopathology