Abstract
Background: The proatlas is derived from the fourth occipital sclerotome in human embryos. It usually fuses with the three upper occipital sclerotomes to form the occipital bone. However, this does not always occur. Manifestations of a partial proatlas structure may persist due to failure of fusion. Clinical considerations: These embryological remnants can induce several symptoms in humans, ranging from mild to severe. On occasion, this structure can go unnoticed until a precipitating traumatic event results in symptoms. Proatlas segmentation abnormalities form bony masses at C1 and the foramen magnum. A number of surgical procedures have been devised to rectify the resulting neural compression and vascular compromise. Discussion: This paper will discuss the development of the proatlas and the resultant anomalies associated with its failure to merge with the occipital sclerotomes to form the occipital bone. In addition, some consideration of comparative anatomy and surgical techniques will be presented.
Original language | English (US) |
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Pages (from-to) | 349-356 |
Number of pages | 8 |
Journal | Child's Nervous System |
Volume | 28 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2012 |
Externally published | Yes |
Keywords
- Atlantic ponticles
- Basilar process
- Bicorunate dens
- Condylus tertius
- Labia of the posterior margin of the foramen magnum
- Median (third) occipital condyle
- Occipital sclerotome
- Ossiculum terminale persistens
- Paracondylar and epitransverse processes
- Partial regressive occipital vertebra
- Rudimentary
ASJC Scopus subject areas
- Pediatrics, Perinatology, and Child Health
- Clinical Neurology