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Nevoid basal cell carcinoma syndrome

โœ Scribed by E. Bohnert; E. G. Jung


Publisher
Springer-Verlag
Year
1989
Tongue
English
Weight
74 KB
Volume
281
Category
Article
ISSN
0340-3696

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## Mutations in the PTCH gene, the human homolog of the Drosophila patched gene, have been found to lead to the autosomal dominant disorder termed Nevoid Basal Cell Carcinoma Syndrome (NBCCS, also called Gorlin Syndrome). Patients display an array of developmental anomalies and are prone to develop

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Nevoid basal cell carcinoma syndrome (NBCC; Gorlin syndrome), an autosomal dominant disorder linked to 9q22.3-q31, and caused by mutations in PTC, the human homologue of the Drosophila patched gene, comprises multiple basal cell carcinomas, keratocysts of the jaw, palmar/plantar pits, spine and rib