| Descriptor English: | Myasthenic Syndromes, Congenital | ||||||
| Descriptor Spanish: |
Síndromes Miasténicos Congénitos
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| Descriptor Portuguese: | Síndromes Miastênicas Congênitas | ||||||
| Descriptor French: | Syndromes myasthéniques congénitaux | ||||||
| Entry term(s): |
Congenital Myasthenia Congenital Myasthenia Gravis Congenital Myasthenias Congenital Myasthenic Syndrome Congenital Myasthenic Syndromes Congenital Myasthenic Syndromes, Postsynaptic Congenital Myasthenic Syndromes, Presynaptic Congenital Slow Channel Myasthenic Syndrome Congenital Slow Channel Myasthenic Syndromes Congenital Slow-Channel Myasthenic Syndrome Congenital Slow-Channel Myasthenic Syndromes Gravi, Congenital Myasthenia Myasthenia Gravis, Congenital Myasthenia, Congenital Myasthenias, Congenital Myasthenic Syndrome, Congenital Myasthenic Syndrome, Congenital, Slow-Channel Myasthenic Syndromes, Congenital, Slow Channel Postsynaptic Congenital Myasthenic Syndrome Postsynaptic Congenital Myasthenic Syndromes Presynaptic Congenital Myasthenic Syndrome Presynaptic Congenital Myasthenic Syndromes Slow Channel Congenital Myasthenic Syndrome Slow Channel Congenital Myasthenic Syndromes Slow-Channel Congenital Myasthenic Syndrome Slow-Channel Congenital Myasthenic Syndromes Syndrome, Congenital Myasthenic Syndromes, Congenital Myasthenic |
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| Tree number(s): |
C10.668.758.800 C16.320.590 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D020294 | ||||||
| Scope 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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| Annotation: | do not confuse with MYASTHENIA GRAVIS, NEONATAL, a transient condition seen in neonates born to myasthenic mothers |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Myasthenia Gravis/congenital (1970-1999) |
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| Public MeSH Note: | 2000 |
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| History Note: | 2000 |
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| Entry Version: | MYASTHENIC SYNDROMES CONGEN |
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| Related: |
Myasthenia Gravis
MeSH | ||||||
| DeCS ID: | 34336 | ||||||
| Unique ID: | D020294 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2000/01/01 | ||||||
| Date of Entry: | 1999/11/08 | ||||||
| Revision Date: | 2020/05/27 |
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Myasthenic Syndromes, Congenital
- Preferred
Myasthenic Syndromes, Congenital, Slow Channel
- Narrower
Congenital Myasthenic Syndromes, Presynaptic
- Narrower
Congenital Myasthenic Syndromes, Postsynaptic
- Narrower
| Concept UI |
M0328231 |
| Scope 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) |
| Preferred term | Myasthenic Syndromes, Congenital |
| Entry term(s) |
Congenital Myasthenia Congenital Myasthenia Gravis Congenital Myasthenias Congenital Myasthenic Syndrome Congenital Myasthenic Syndromes Gravi, Congenital Myasthenia Myasthenia Gravis, Congenital Myasthenia, Congenital Myasthenias, Congenital Myasthenic Syndrome, Congenital Syndrome, Congenital Myasthenic Syndromes, Congenital Myasthenic |
| Concept UI |
M0337366 |
| Preferred term | Myasthenic Syndromes, Congenital, Slow Channel |
| Entry term(s) |
Congenital Slow Channel Myasthenic Syndrome Congenital Slow Channel Myasthenic Syndromes Congenital Slow-Channel Myasthenic Syndrome Congenital Slow-Channel Myasthenic Syndromes Myasthenic Syndrome, Congenital, Slow-Channel Slow Channel Congenital Myasthenic Syndrome Slow Channel Congenital Myasthenic Syndromes Slow-Channel Congenital Myasthenic Syndrome Slow-Channel Congenital Myasthenic Syndromes |
| Concept UI |
M0337368 |
| Preferred term | Congenital Myasthenic Syndromes, Presynaptic |
| Entry term(s) |
Presynaptic Congenital Myasthenic Syndrome Presynaptic Congenital Myasthenic Syndromes |
| Concept UI |
M0337367 |
| Preferred term | Congenital Myasthenic Syndromes, Postsynaptic |
| Entry term(s) |
Postsynaptic Congenital Myasthenic Syndrome Postsynaptic Congenital Myasthenic Syndromes |
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