paralysie périodique avec neuropathie motrice distale tardive
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.
SNOMEDCT-BE (disorder) / 774154008
SNOMEDCT-BE (which responds to acetazolamide treatment) associated with later-onset chronic slowly progressive distal axonal neuropathy. / 774154008