Abstract
Nevoid basal cell carcinoma syndrome (NBCCS) is characterised by skeletal anomalies, cutaneous basal cell carcinomas and multiple keratocysts. NBCCS is an autosomal dominant disorder, but can have a variable phenotypic penetration. NBCCS can also arise spontaneously. The prevalence is 1:60.000 and 50-65% of patients with NBCCS have affected family members. A recently diagnosed patient is presented and the manifestations of the syndrome are discussed
Original language | Dutch |
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Pages (from-to) | 298-301 |
Journal | Nederlands tijdschrift voor tandheelkunde |
Volume | 112 |
Issue number | 8 |
Publication status | Published - 2005 |