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What is Myasthenic syndrome, congenital, slow-channel?

What is Myasthenic syndrome, congenital, slow-channel?

  • Myasthenic syndrome, congenital, slow-channel: 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.

Myasthenic syndrome, congenital, slow-channel: Introduction

Types of Myasthenic syndrome, congenital, slow-channel:

Broader types of Myasthenic syndrome, congenital, slow-channel:

How serious is Myasthenic syndrome, congenital, slow-channel?

Prognosis of Myasthenic syndrome, congenital, slow-channel: severity of symptoms is variable and the extent of muscle groups involved is also variable; some become wheelchair dependent during childhood

What causes Myasthenic syndrome, congenital, slow-channel?

Causes of Myasthenic syndrome, congenital, slow-channel: see causes of Myasthenic syndrome, congenital, slow-channel

What are the symptoms of Myasthenic syndrome, congenital, slow-channel?

Symptoms of Myasthenic syndrome, congenital, slow-channel: see symptoms of Myasthenic syndrome, congenital, slow-channel

Myasthenic syndrome, congenital, slow-channel: Testing

Diagnostic testing: see tests for Myasthenic syndrome, congenital, slow-channel.

Misdiagnosis: see misdiagnosis and Myasthenic syndrome, congenital, slow-channel.

How is it treated?

Doctors and Medical Specialists for Myasthenic syndrome, congenital, slow-channel: Medical Geneticist ; see also doctors and medical specialists for Myasthenic syndrome, congenital, slow-channel.
Treatments for Myasthenic syndrome, congenital, slow-channel: see treatments for Myasthenic syndrome, congenital, slow-channel

Name and Aliases of Myasthenic syndrome, congenital, slow-channel

Main name of condition: Myasthenic syndrome, congenital, slow-channel

Other names or spellings for Myasthenic syndrome, congenital, slow-channel:

myasthenic syndrome, congenital, postsynaptic slow-channel, myasthenic syndrome, congenital type IIa, CMS2A, CMSIIa, SCCMS

 

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