Infantile progressive bulbar palsy
In this article, we will address the topic of Infantile progressive bulbar palsy from different perspectives and points of view. We will analyze its importance, impact and relevance today, as well as its evolution over time. We will examine the different opinions and positions on the matter, with the aim of offering a comprehensive and complete vision of Infantile progressive bulbar palsy. To do this, we will rely on data, research and testimonies that allow us to deepen our knowledge and understanding of this topic. With a critical and reflective approach, we will explore the implications and consequences of Infantile progressive bulbar palsy in society, culture and the world in general.
| Infantile progressive bulbar palsy | |
|---|---|
| Specialty | Neurology |
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
- ^ 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. Retrieved 5 December 2017.
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