| Descriptor English: | Bulbar Palsy, Progressive | ||||||
| Descriptor Spanish: |
Parálisis Bulbar Progresiva
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| Descriptor Portuguese: | Paralisia Bulbar Progressiva | ||||||
| Descriptor French: | Paralysie bulbaire progressive | ||||||
| Entry term(s): |
Bulbar Palsies Bulbar Palsies, Progressive Bulbar Palsy Bulbar Palsy, Progressive, Of Childhood Bulbar Paralyses Bulbar Paralysis Childhood Progressive Bulbar Palsy Fazio-Londe Disease Fazio-Londe Syndrome Fazio-Londe's Disease Fazio-Londe's Syndrome Palsies, Bulbar Palsies, Progressive Bulbar Palsy, Bulbar Palsy, Progressive Bulbar Paralysis, Bulbar Progressive Bulbar Palsies Progressive Bulbar Palsy Progressive Bulbar Palsy of Childhood |
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| Tree number(s): |
C10.574.562.300 C10.668.467.300 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D010244 | ||||||
| Scope note: | 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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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital 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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| Public MeSH Note: | 2000; see PARALYSIS, BULBAR 1966-1999 |
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| History Note: | 2000(1966) |
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| DeCS ID: | 10433 | ||||||
| Unique ID: | D010244 | ||||||
| NLM Classification: | WL 310 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2000/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2016/06/08 |
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Bulbar Palsy, Progressive
- Preferred
Bulbar Palsy
- Broader
Childhood Progressive Bulbar Palsy
- Narrower
| Concept UI |
M0015879 |
| Scope note | 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) |
| Preferred term | Bulbar Palsy, Progressive |
| Entry term(s) |
Bulbar Palsies, Progressive Palsies, Progressive Bulbar Palsy, Progressive Bulbar Progressive Bulbar Palsies Progressive Bulbar Palsy |
| Concept UI |
M000618614 |
| Preferred term | Bulbar Palsy |
| Entry term(s) |
Bulbar Palsies Bulbar Paralyses Bulbar Paralysis Palsies, Bulbar Palsy, Bulbar Paralysis, Bulbar |
| Concept UI |
M0337043 |
| Preferred term | Childhood Progressive Bulbar Palsy |
| Entry term(s) |
Bulbar Palsy, Progressive, Of Childhood Fazio-Londe Disease Fazio-Londe Syndrome Fazio-Londe's Disease Fazio-Londe's Syndrome Progressive Bulbar Palsy of Childhood |
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