Congenital myasthenic syndrome
MONDO:0018940Congenital myasthenic syndrome (CMS) is a group of genetic disorders of impaired neuromuscular transmission at the motor endplate characterized by fatigable muscle weakness.
Also known as: CMS, Congenital Myasthenic Syndromes, myasthenic syndrome, congenital, congenital MG, congenital myasthenia, erb-Goldflam syndrome, familial limb-girdle myasthenia, myasthenia gravis congenital
5 clinical trials for this condition and its sub-types.
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Congenital myasthenic syndrome 10
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Congenital myasthenic syndrome 17
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Congenital myasthenic syndrome 8
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Congenital myasthenic syndrome 9
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Congenital myasthenic syndrome 11
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Congenital myasthenic syndrome 12
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Congenital myasthenic syndrome 13
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Congenital myasthenic syndrome 14
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Congenital myasthenic syndrome 15
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Congenital myasthenic syndrome 16
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Congenital myasthenic syndrome 18
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Congenital myasthenic syndrome 19
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Congenital myasthenic syndrome 1A
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Congenital myasthenic syndrome 20
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Congenital myasthenic syndrome 21
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Congenital myasthenic syndrome 2A
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Congenital myasthenic syndrome 2C
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Congenital myasthenic syndrome 3A
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Congenital myasthenic syndrome 3B
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Congenital myasthenic syndrome 3C
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