We report three new cases of sub-occipital Pott disease (C1-C2) seen at the University Hospital of Cocody (Abidjan) with their clinical features. In the first case, the mode of revelation was original and unique: an incomplete Brown-Séquard syndrome. The second case provided warning about the dangers of self-medication and untimely antibiotic usage. The third case informed about the imperative to make the differential diagnosis. The histological or bacteriological arguments led to the diagnosis in the first two cases, associated with a visceral localization. Therapeutic evidence was required in the third case. The sub-occipital Pott's disease remains a rare localization.
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