Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination

@article{Warner1996ClinicalPO,
  title={Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination},
  author={Laura E. Warner and Max J Hilz and Stanley H. Appel and James M. Killian and Edwin H. Kolodny and George Karpati and Stirling Carpenter and Gordon V Watters and Calvin Wheeler and David Witt and Adria L Bodell and Eva Nelis and Christine Van Broeckhoven and James R Lupski},
  journal={Neuron},
  year={1996},
  volume={17},
  pages={451-460}
}
Hereditary demyelinating peripheral neuropathies consist of a heterogeneous group of genetic disorders that includes hereditary neuropathy with liability to pressure palsies (HNPP), Charcot-Marie-Tooth disease (CMT), Dejerine-Sottas syndrome (DSS), and congenital hypomyelination (CH). The clinical classification of these neuropathies into discrete categories can sometimes be difficult because there can be both clinical and pathologic variation and overlap between these disorders. We have… CONTINUE READING
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