Hypoplastic occipital condyle and third occipital condyle: Review of their dysembryology. Issue 8 (21st January 2013)

• Record Type: Journal Article
• Authors: Tubbs, R. Shane; Lingo, Patrick Ryan; Mortazavi, Martin M.; Cohen‐gadol, Aaron A.
• Is Part Of: Clinical anatomy. Volume 26:Issue 8(2013:Nov.)
• Page Start: 928
• Page End: 932
• Publication Date: 2013-01-21
• Subjects: Anatomy -- Periodicals; Anatomy -- Periodicals; 611
• DOI: 10.1002/ca.22205
• Languages: English
• ISSNs: 0897-3806

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Disruption or embryologic derailment of the normal bony architecture of the craniovertebral junction (CVJ) may result in symptoms. As studies of the embryology and pathology of hypoplasia of the occipital condyles and third occipital condyles are lacking in the literature, the present review was performed. Standard search engines were accessed and queried for publications regarding hypoplastic occipital condyles and third occipital condyles. The literature supports the notion that occipital condyle hypoplasia and a third occipital condyle are due to malformation or persistence of the proatlas, respectively. The Pax‐1 gene is most likely involved in this process. Clinically, condylar hypoplasia may narrow the foramen magnum and lead to lateral medullary compression. Additionally, this maldevelopment can result in transient vertebral artery compression secondary to posterior subluxation of the occiput. Third occipital condyles have been associated with cervical canal stenosis, hypoplasia of the dens, transverse ligament laxity, and atlanto‐axial instability causing acute and chronic spinal cord compression. Treatment goals are focused on craniovertebral stability. A better understanding of the embryology and pathology related to CVJ anomalies is useful to the clinician treating patients presenting with these entities. Clin. Anat. 26:928–932, 2013. © 2013 Wiley Periodicals, Inc.</p> </abstract>