Gorlin syndrome (nevoid basal cell carcinoma syndrome);Síndrome de Gorlin (síndrome nevoide basocelular)

Archivos de la Sociedad Espanola de Oftalmologia

Volumn 83, Issue 5, 2008, Pages 321-324

  De Domingo Barón, Begoña ^a,b   Gonzalez F ^a   Lorenzo, P ^a  

^a University Hospital of Santiago de Compostela   (Spain)

^b NONE   (Spain)

Author keywords

Ameloblastoma; Basal cell carcinoma; Gorlin syndrome; Nevoid basal cell carcinoma syndrome; PTCH gene

Indexed keywords

AGED; ARTICLE; BASAL CELL NEVUS SYNDROME; CASE REPORT; EYELID TUMOR; HUMAN; MALE; PATHOLOGY;

AGED; BASAL CELL NEVUS SYNDROME; EYELID NEOPLASMS; HUMANS; MALE;

EID: 45849123848     PISSN: 03656691     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Ragge NK, Salt A, O Collin JR, Michalski A, Farndon PA. Gorlin syndrome: the PTCH gene links ocular developmental defects and tumour formation. Br J Ophthalmol 2005; 89: 988-991.
2. Anh SG, Lim YS, Kim DK, Lee SH, Yoon JH. Nevoid basal cell carcinoma syndrome: a retrospective analysis of 33 affected korean individuals. Int J Oral Maxillofac Surg 2004; 33: 458-462.
3. Lo Muzio L, Nocini P, Bucci P, Pannone G, Consolo U, Procaccini M. Early diagnosis of nevoid basal cell carcinoma syndrome. J Am Dent Assoc 1999; 130: 669-674.
4. Honavar SG, Shields JA, Shields CL, Eagle RC Jr, Demirci H, Mahmood EZ. Basal cell carcinoma of the eyelid associated with Gorlin-Goltz syndrome. Ophthalmology 2001; 108: 1115-1123.
5. Scott A, Strouthidis NG, Robson AG, Forsyth J, Maher ER, Schlottmann PG, et al. Bilateral epiretinal membranes in Gorlin syndrome associated with a novel PTCH mutation. Am J Ophthalmol 2007; 143: 346-348.