Medicine:Infantile progressive bulbar palsy

From HandWiki
Revision as of 23:56, 4 February 2024 by Sherlock (talk | contribs) (linkage)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Infantile progressive bulbar palsy
SpecialtyNeurology

Infantile progressive bulbar palsy is a rare type of progressive 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) and Brown–Vialetto–Van Laere syndrome (BVVL).[2]

References

  1. Wilson, John Eastman (1909) (in en). Diseases of the nervous system. Boericke & Runyon. p. 296. https://archive.org/details/diseasesnervous02wilsgoog. Retrieved 5 December 2017. "Infantile progressive bulbar palsy." 
  2. Piña-Garza, J. Eric (2013) (in en). Fenichel's Clinical Pediatric Neurology E-Book: A Signs and Symptoms Approach. Elsevier Health Sciences. p. 328. ISBN 978-1455748129. https://books.google.com/books?id=jkMPxMpshlEC&q=Infantile+progressive+bulbar+palsy. Retrieved 5 December 2017.