Number of the records: 1
syndrómy myastenické vrodené
Record number d020294 Date 06.06.2025 Type M Topical term syndrómy myastenické vrodené Other term English (Pseudonym) Congenital Slow-Channel Myasthenic Syndrome
English (Pseudonym) Myasthenic Syndromes, Congenital, Slow Channel
English (Pseudonym) Postsynaptic Congenital Myasthenic Syndrome
English (Pseudonym) Presynaptic Congenital Myasthenic Syndrome
English (Pseudonym) Slow-Channel Congenital Myasthenic Syndrome
Slovak (Pseudonym) myasténia vrodená
Slovak (Pseudonym) myasténia kongenitálna
Slovak (Pseudonym) syndrómy myastenické kongenitálne
Slovak (Pseudonym) syndróm myastenický kongenitálny
Slovak (Pseudonym) syndrómy myastenické vrodené, postsynaptické
Slovak (Pseudonym) syndrómy myastenické vrodené, presynaptické
Slovak (Pseudonym) syndrómy myastenické vrodené, pomalých kanálov
Slovak (Pseudonym) syndrómy myastenické kongenitálne, pomalých kanálov
Slovak (Pseudonym) myasténia gravis, vrodená
Slovak (Pseudonym) myasthenia gravis, vrodená
See also (Skutočné meno) myasthenia gravis
UDC C10.668.758.800C16.320.590 Note A heterogeneous group of disorders characterized by a congenital defect in neuromuscular transmission at the NEUROMUSCULAR JUNCTION. This includes presynaptic, synaptic, and postsynaptic disorders (that are not of autoimmune origin). The majority of these diseases are caused by mutations of various subunits of the nicotinic acetylcholine receptor (RECEPTORS, NICOTINIC) on the postsynaptic surface of the junction. (From Arch Neurol 1999 Feb;56(2):163-7) 
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Number of the records: 1