Severe myoclonic epilepsy and mitochondrial cytopathy

@article{CastroGago2014SevereME,
  title={Severe myoclonic epilepsy and mitochondrial cytopathy},
  author={M. Castro‐Gago and J. Eir{\'i}s-Pu{\~n}al and J. M. Martin{\'o}n S{\'a}nchez and A. Rodr{\'i}guez-N{\'u}{\~n}ez and J. H. Herranz Fern{\'a}ndez},
  journal={Child’s Nervous System},
  year={2014},
  volume={13},
  pages={570-571}
}
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References

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Severe myoclonic epilepsy associated with mitochondrial cytopathy
TLDR
Thorough diagnostic analysis in severe myoclonic epilepsy cases is called for with a view to elucidation of a possible metabolic aetiology. Expand
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The six crucial clinical issues are identified are to identify non-epileptic attacks, identify benign and malignant syndromes, use predicted prognosis to guide management, and identify and manage coexisting disabilities. Expand
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