Difference between revisions of "Nevoid basal cell carcinoma syndrome"
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'''Nevoid basal cell carcinoma syndrome''' | '''Nevoid basal cell carcinoma syndrome''', also ''Gorlin syndrome''' and ''Gorlin-Goltz syndrome''', is a constellation of findings due to an autosomal dominant genetic mutation. | ||
Features:<ref name=Ref_Derm435>{{Ref Derm|435}}</ref> | |||
*Basal cell carcinoma. | *Basal cell carcinoma. | ||
*[[Keratocystic odontogenic tumour]]. | |||
*Bony abnormalities: bifid ribs, scoliosis + others. | |||
*Falx cerebri calcification. | |||
*Characteristic faces. | |||
==See also== | ==See also== | ||
Revision as of 20:38, 10 September 2010
Nevoid basal cell carcinoma syndrome, also Gorlin syndrome and Gorlin-Goltz syndrome, is a constellation of findings due to an autosomal dominant genetic mutation.
Features:[1]
- Basal cell carcinoma.
- Keratocystic odontogenic tumour.
- Bony abnormalities: bifid ribs, scoliosis + others.
- Falx cerebri calcification.
- Characteristic faces.
See also
References
- ↑ Busam, Klaus J. (2009). Dermatopathology: A Volume in the Foundations in Diagnostic Pathology Series (1st ed.). Saunders. pp. 435. ISBN 978-0443066542.