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Infantile progressive bulbar palsy

From Wikipedia, the free encyclopedia
Medical condition
Infantile progressive bulbar palsy
SpecialtyNeurology

Infantile progressive bulbar palsy is a rare type ofprogressive bulbar palsy that occurs in children. The disease exists in both rapid and slow onsets, and involves inflammation of the gray matter of the bulb.[1] Infantile PBP is a disease that manifests itself in two forms:Fazio–Londe syndrome (FL) andBrown–Vialetto–Van Laere syndrome (BVVL).[2]

References

[edit]
  1. ^Wilson, John Eastman (1909).Diseases of the nervous system. Boericke & Runyon. p. 296. Retrieved5 December 2017.Infantile progressive bulbar palsy.
  2. ^Piña-Garza, J. Eric (2013).Fenichel's Clinical Pediatric Neurology E-Book: A Signs and Symptoms Approach. Elsevier Health Sciences. p. 328.ISBN 978-1455748129. Retrieved5 December 2017.
Diseases of thenervous system, primarilyCNS
Inflammation
Brain
Brain andspinal cord
Brain/
encephalopathy
Degenerative
Extrapyramidal and
movement disorders
Dementia
Mitochondrial disease
Demyelinating
Episodic/
paroxysmal
Seizures andepilepsy
Headache
Cerebrovascular
Other
CSF
Other
Both/either
Degenerative
SA
MND
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