Infantile progressive bulbar palsy
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|Infantile progressive bulbar palsy|
|Mutations in SLC52A2 in Brown-Vialetto-Van Laere syndrome a) Predicted transmembrane domains in RFVT2 b)structural conservation of relevant amino acid residues in RFVT2 across species and in RFVT1 and RFVT3|
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.
Infantile PBP is a disease that manifests itself in two forms: Fazio–Londe syndrome (FL) and Brown–Vialetto–Van Laere syndrome (BVVL).
- ↑ Wilson, John Eastman (1909). Diseases of the nervous system. Boericke & Runyon. p. 296. Retrieved 5 December 2017.
Infantile progressive bulbar palsy.
- ↑ 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. Archived from the original on 18 July 2021. Retrieved 5 December 2017.