CMS IIa (medical condition): A rare disorder involving progressive muscle wasting and weakness of variable severity depending on the exact origin of the genetic defect. The problem arises from defective processes at the junction of nerve and muscle cells.
See also:
Myasthenic syndrome, congenital, slow-channel:
»Introduction: Myasthenic syndrome, congenital, slow-channel
»Symptoms of Myasthenic syndrome, congenital, slow-channel
CMS IIa: Another name for Myasthenic syndrome, congenital, slow-channel (or close medical condition association).
»Introduction: Myasthenic syndrome, congenital, slow-channel
»Symptoms of Myasthenic syndrome, congenital, slow-channel
Some of the symptoms of CMS IIa incude:
See full list of 10 symptoms of CMS IIa (Myasthenic syndrome, congenital, slow-channel)
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