Genetic diagnoses in Charcot–Marie–Tooth disease (CMT) and related disorders in patients attending a specialist CMT clinic in the UK (inherited neuropathy.

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Presentation transcript:

Genetic diagnoses in Charcot–Marie–Tooth disease (CMT) and related disorders in patients attending a specialist CMT clinic in the UK (inherited neuropathy clinic, National Hospital for Neurology and Neurosurgery, Queen Square).17 It can be seen that for the majority of patients with CMT2, hereditary sensory neuropathy (HSN) and hereditary motor neuropathy (HMN) the underlying genetic defect is unknown. Genetic diagnoses in Charcot–Marie–Tooth disease (CMT) and related disorders in patients attending a specialist CMT clinic in the UK (inherited neuropathy clinic, National Hospital for Neurology and Neurosurgery, Queen Square).17 It can be seen that for the majority of patients with CMT2, hereditary sensory neuropathy (HSN) and hereditary motor neuropathy (HMN) the underlying genetic defect is unknown. BSCL, Berardinelli-Seip congenital lipodystrophy; GARS, glycyl tRNA synthetase; HSPB8, heat shock protein 22kDa protein 8; MFN, mitofusin 2; MPZ, myelin protein zero; NGFB, nerve growth factor β; PMP, peripheral myelin protein; SPTLC, serine palmitoyltransferase, long-chain; SMN, survival of motor neuron. Alexander M Rossor et al. Pract Neurol 2015;15:187-198 ©2015 by BMJ Publishing Group Ltd