## Abstract Sixteen infants, aged 3 to 81/2 months, were studied close to the onset of a myoclonic syndrome akin to that normally called __infantile spasms__ with hypsarrhythmia. None were found to have the clinical and laboratory characteristics common to the syndrome, however: none showed regress
β¦ LIBER β¦
Benign myoclonus of early infancy or Fejerman syndrome
β Scribed by Bernardo Dalla Bernardina
- Book ID
- 109111297
- Publisher
- Wiley (Blackwell Publishing)
- Year
- 2009
- Tongue
- English
- Weight
- 121 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0013-9580
No coin nor oath required. For personal study only.
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Opsoclonus myoclonus syndrome (OMS) is a rare disease characterized by opsoclonus, an eye movement disorder causing involuntary, chaotic saccades in all directions, and arrhythmic action myoclonus often involving the trunk, limbs, and head. 1 Cerebellar dysfunction with dysarthria and ataxia as well