Cervical Myelopathy due to Congenital Atlanto-axial Dislocation

Authors

  • PVS Rana Department of Medicine Manipal Teaching Hospital Manipal College of Medical Sciences Pokhara
  • Mohit P. Shetti Department of Medicine Manipal Teaching Hospital Manipal College of Medical Sciences Pokhara
  • Lekhjung Thapa Department of Medicine Manipal Teaching Hospital Manipal College of Medical Sciences Pokhara,

DOI:

https://doi.org/10.3126/njn.v2i1.19998

Keywords:

Atlanto-axial joint (AAJ), Basilar invagination, Cervical myelopathy, Congenital atlanto-axial dislocation (CAAD), Craniovertebral junction (CVJ) anomalies, Syringomyelia

Abstract

Five cases of atlanto-axial dislocation (AAD) are reported with emphasis on their clinical presentation and literature is reviewed. The first patient had gross AAD and presented as progressive myelopathy. The second patient had AAD with occipitalization of atlas, Chiari malformation and syringomyelia where headache was the only presenting symptom. The third patient with AAD, had occipitalization of atlas and fusion of cervical second and third (C2- C3) vertebrae. She presented with peculiar sensation over forehead. Detection of pathologically brisk tendon reflexes in the lower limbs and extensor plantar response led to further investigation and diagnosis of the condition. The fourth patient had AAD and advanced spondylotic changes. His symptoms manifested after injury and then progressed gradually leading to quadriplegia. The fifth case presented with nuchal and occipital neuralgia, paresthesia in hands and brisk reflexes. X-ray cervical spine showed unfused, separate but fully developed odontoid process and AAD. All these patients represented congenital AAD.

 Nepal Journal of Neuroscience, Volume 2, Number 1, 2005, Page 71-76

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Published

2005-01-31

How to Cite

1.
Rana P, Shetti MP, Thapa L. Cervical Myelopathy due to Congenital Atlanto-axial Dislocation. Nep J Neurosci [Internet]. 2005 Jan. 31 [cited 2024 Apr. 16];2(1):71-6. Available from: https://www.nepjol.info/index.php/NJN/article/view/19998

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Section

Original Articles