Myasthenic Syndromes, Congenital

"Myasthenic Syndromes, Congenital" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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)

Descriptor ID	D020294
MeSH Number(s)	C10.668.758.800 C16.320.590
Concept/Terms	Myasthenic Syndromes, Congenital Myasthenic Syndromes, Congenital Congenital Myasthenic Syndrome Myasthenic Syndrome, Congenital Syndrome, Congenital Myasthenic Syndromes, Congenital Myasthenic Congenital Myasthenic Syndromes Myasthenia Gravis, Congenital Congenital Myasthenia Gravis Gravi, Congenital Myasthenia Congenital Myasthenic Syndromes, Presynaptic Congenital Myasthenic Syndromes, Presynaptic Presynaptic Congenital Myasthenic Syndromes Myasthenic Syndromes, Congenital, Slow Channel Myasthenic Syndromes, Congenital, Slow Channel Slow-Channel Congenital Myasthenic Syndromes Slow Channel Congenital Myasthenic Syndromes Myasthenic Syndrome, Congenital, Slow-Channel Congenital Slow-Channel Myasthenic Syndromes Congenital Slow Channel Myasthenic Syndromes Congenital Myasthenic Syndromes, Postsynaptic Congenital Myasthenic Syndromes, Postsynaptic Postsynaptic Congenital Myasthenic Syndromes

Below are MeSH descriptors whose meaning is more general than "Myasthenic Syndromes, Congenital".

Diseases [C]
Nervous System Diseases [C10]
Neuromuscular Diseases [C10.668]
Neuromuscular Junction Diseases [C10.668.758]
Myasthenic Syndromes, Congenital [C10.668.758.800]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Genetic Diseases, Inborn [C16.320]
Myasthenic Syndromes, Congenital [C16.320.590]

Below are MeSH descriptors whose meaning is related to "Myasthenic Syndromes, Congenital".

Below are MeSH descriptors whose meaning is more specific than "Myasthenic Syndromes, Congenital".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Myasthenic Syndromes, Congenital" by people in this website by year, and whether "Myasthenic Syndromes, Congenital" was a major or minor topic of these publications.

To see the data from this visualization as text, click here.