Table 6 Comparison of the craniocervical junction abnormalities between genetic skeletal disorder patients with and without CNS injury.

From: Identification of clinical and radiographic predictors of central nervous system injury in genetic skeletal disorders

Craniocervical junction abnormalities

CNS injury

n (%)

No CNS injury

n (%)

p*

OR

(95% CI)

Os odontoideum

11/71 (15.5)

9/201 (4.5)

0.006

4.2 (1.4–11.1)

Basilar impression/invagination

15/71 (21.1)

20/201 (10.0)

0.016

2.4 (1.1–5.3)

Narrowed foramen magnum

14/71 (19.7)

20/201 (10.0)

0.032

2.2 (1.0–5.0)

Spinal canal stenosis at C2

59/71 (83.1)

155/201 (77.1)

0.290

1.5 (0.7–3.2)

Atlanto-odontoid instability

6/71 (8.5)

10/201 (5.0)

0.377

1.8 (0.5–5.6)

Cervical spinal cord compression

17/71 (23.9)

41/201 (20.4)

0.531

1.2 (0.6–2.4)

Atlanto-occipital instability

3/71 (4.2)

6/201 (3.0)

0.701

1.4 (0.2–6.9)

Basio-occipital hypoplasia

41/71 (57.7)

127/201 (60.7)

0.768

0.9 (0.5–1.6)

Terminal bone at C2

2/71 (2.8)

4/201 (2.0)

1.000

0.9 (0.1–5.4)

Platybasia

1/71 (1.4)

4/201 (2.0)

1.000

0.7 (0.1–7.3)

  1. CNS central nervous system, OR odds ratio, CI confidence interval.
  2. *X2 test or Fisher’s exact test.