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Up to: Hereditary neurological disease · Developmental defect during embryogenesis · Hereditary neoplastic syndrome · Autosomal dominant disease · Neurocutaneous syndrome

Nevoid basal cell carcinoma syndrome

A rare hereditary disorder due to autosomal dominant transmission with hamartosis characterized by multiple early-onset basal cell carcinoma (BCC), multiple jaw keratocysts and skeletal abnormalities.

5 trials tagged with this condition →