A very rare syndrome with characteristics of the association of Mobius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic.

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syndrome de Moebius-neuropathie axonale-hypogonadisme hypogonadotrope

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

A rare genetic neuromuscular disease with characteristics of acute episodic muscle weakness in upper and lower extremities (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy.

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paralysie périodique avec neuropathie motrice distale tardive

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A rare hereditary motor and sensory neuropathy with characteristics of intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both axonal degeneration and demyelination without onion bulbs in nerve biopsies

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maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante D

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https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

presynaptic ending

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

terminaison présynaptique

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http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

pre-synaptic neuron [ presynaptic neuron ]

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

neurone présynaptique [ neurone pré-synaptique ]