An extremely rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by a CMT neuropathy associated with developmental delay, self-abusive behavior, dysmorphic features and vestibular Schwannoma. Motor nerve c

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maladie de Charcot-Marie-Tooth intermédiaire autosomique récessive type B

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damage to cranial nerves

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atteinte des nerfs craniens

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Compression of optic nerve Haemorrhage in optic nerve sheath Ischaemic optic neuropathy

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Compression du nerf optique Hémorragie de la gaine du nerf optique Neuropathie optique ischémique

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D'autres ont cherché : nerve damage neuropathy damage to cranial nerves quiet nerve paralysis silent neuritis silent neuropathy neuropathy nerve damage

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Date index: 2021-11-21