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Last uploaded:
January 16, 2025
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| Id | http://purl.bioontology.org/ontology/MESH/D010244
http://purl.bioontology.org/ontology/MESH/D010244
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|---|---|
| Preferred Name | Bulbar Palsy, Progressive |
| Definitions |
A motor neuron disease marked by progressive weakness of the muscles innervated by cranial nerves of the lower brain stem. Clinical manifestations include dysarthria, dysphagia, facial weakness, tongue weakness, and fasciculations of the tongue and facial muscles. The adult form of the disease is marked initially by bulbar weakness which progresses to involve motor neurons throughout the neuroaxis. Eventually this condition may become indistinguishable from AMYOTROPHIC LATERAL SCLEROSIS. Fazio-Londe syndrome is an inherited form of this illness which occurs in children and young adults. (Adams et al., Principles of Neurology, 6th ed, p1091; Brain 1992 Dec;115(Pt 6):1889-1900)
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| Synonyms |
Syndrome, Fazio-Londe
Disease, Fazio-Londe's
Fazio Londe's Disease
Progressive Bulbar Palsies
Palsy, Bulbar
Bulbar Palsies, Progressive
Fazio-Londe's Disease
Paralysis, Bulbar
Bulbar Paralyses
Childhood Progressive Bulbar Palsy
Fazio Londe's Syndrome
Fazio Londe Syndrome
Syndrome, Fazio-Londe's
Fazio-Londe Disease
Fazio-Londe Syndrome
Progressive Bulbar Palsy of Childhood
Bulbar Paralysis
Palsies, Progressive Bulbar
Bulbar Palsy, Progressive, Of Childhood
Bulbar Palsy
Palsies, Bulbar
Bulbar Palsies
Fazio-Londe's Syndrome
Palsy, Progressive Bulbar
Fazio Londe Disease
Disease, Fazio-Londe
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | A motor neuron disease marked by progressive weakness of the muscles innervated by cranial nerves of the lower brain stem. Clinical manifestations include dysarthria, dysphagia, facial weakness, tongue weakness, and fasciculations of the tongue and facial muscles. The adult form of the disease is marked initially by bulbar weakness which progresses to involve motor neurons throughout the neuroaxis. Eventually this condition may become indistinguishable from AMYOTROPHIC LATERAL SCLEROSIS. Fazio-Londe syndrome is an inherited form of this illness which occurs in children and young adults. (Adams et al., Principles of Neurology, 6th ed, p1091; Brain 1992 Dec;115(Pt 6):1889-1900) |
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| altLabel |
Syndrome, Fazio-Londe
Disease, Fazio-Londe's
Fazio Londe's Disease
Progressive Bulbar Palsies
Palsy, Bulbar
Bulbar Palsies, Progressive
Fazio-Londe's Disease
Paralysis, Bulbar
Bulbar Paralyses
Childhood Progressive Bulbar Palsy
Fazio Londe's Syndrome
Fazio Londe Syndrome
Syndrome, Fazio-Londe's
Fazio-Londe Disease
Fazio-Londe Syndrome
Progressive Bulbar Palsy of Childhood
Bulbar Paralysis
Palsies, Progressive Bulbar
Bulbar Palsy, Progressive, Of Childhood
Bulbar Palsy
Palsies, Bulbar
Bulbar Palsies
Fazio-Londe's Syndrome
Palsy, Progressive Bulbar
Fazio Londe Disease
Disease, Fazio-Londe
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| prefLabel |
Bulbar Palsy, Progressive
|
| TH |
OMIM (2013)
NLM (2000)
NLM (2023)
NLM (1966)
UNK (19XX)
|
| notation |
D010244
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| DX |
20000101
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| Machine permutation |
2000; see PARALYSIS, BULBAR 1966-1999
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| MN |
C10.574.562.300
C10.668.467.300
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| MMR |
20220714
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| Mapped from | |
| AQL |
BL CF CI CL CN CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI
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| HN |
2000(1966)
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| subClassOf | |
| Semantic type UMLS property | |
| DC |
1
|
| MDA |
19990101
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| type | |
| tui |
T047
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| cui |
C0393540
C4082299
C0030442
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| Inverse of AQ |
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| TERMUI |
T372094
T365782
T001115762
T001114240
T030275
T030274
T001114241
T372095
T812345
T001115763
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