48,830
edits
Difference between revisions of "Nevoid basal cell carcinoma syndrome"
Jump to navigation
Jump to search
Nevoid basal cell carcinoma syndrome (view source)
Revision as of 01:54, 31 May 2012
, 01:54, 31 May 2012+gene
(+images) |
(+gene) |
||
| Line 1: | Line 1: | ||
'''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> | ||