Nevoid basal cell carcinoma syndrome: Difference between revisions

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'''Nevoid basal cell carcinoma syndrome''', also '''Gorlin syndrome''' and '''Gorlin-Goltz syndrome''', is a constellation of findings due to an autosomal dominant genetic mutation.
'''Nevoid basal cell carcinoma syndrome''', also '''Gorlin syndrome''' and '''Gorlin-Goltz syndrome''', is a constellation of findings due to an autosomal dominant genetic mutation. The gene is ''patched'' and abbreviated ''PTCH1''.<ref name=omim601309>{{OMIM|601309}}</ref>


Features:<ref name=Ref_Derm435>{{Ref Derm|435}}</ref>
Features:<ref name=Ref_Derm435>{{Ref Derm|435}}</ref>
Retrieved from "https://librepathology.org/wiki/Nevoid_basal_cell_carcinoma_syndrome"