| Literature DB >> 28612426 |
Mohammadali M Shoja1, Jaspreet Johal2, W Jerry Oakes3, R Shane Tubbs2,4.
Abstract
Although the Chiari malformations are well-studied and described developmental anomalies, there remains some incongruity in regards to their underlying etiologies. A number of theories have been proposed with the purpose of accounting for the embryology and pathogenesis of the Chiari I and II malformations and their associated complications and clinical syndromes. The present review aims to review the pertinent literature for all of the main theories that have been proposed, and outline their validity and relevance to our contemporary understanding of these anomalies. Clin. Anat. 31:202-215, 2018.Entities:
Keywords: Arnold-Chiari malformation; cerebrospinal fluid pressure; etiology; hydrocephalus; mechanism; syringomyelia
Mesh:
Year: 2017 PMID: 28612426 DOI: 10.1002/ca.22939
Source DB: PubMed Journal: Clin Anat ISSN: 0897-3806 Impact factor: 2.414