A case of Gorlin syndrome like phenotype with multiple infundibulocystic basal cell carcinomas in a moniliform blepharosis arrangement-Reference-Cited by-同舟云学术

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A case of Gorlin syndrome like phenotype with multiple infundibulocystic basal cell carcinomas in a moniliform blepharosis arrangement

Published:2023-04 Issue: Volume:34 Page:27-31
ISSN:2352-5126
Container-title:JAAD Case Reports
language:en
Short-container-title:JAAD Case Reports

Author:

Petrosian David,Reiter Paloma,Rozenberg Suzanne Sirota,Petrosian Sergey

Publisher

Elsevier BV

Subject

Dermatology

Reference10 articles.

1. Nevoid basal cell carcinoma syndrome or multiple hereditary infundibulocystic basal cell carcinoma syndrome?;Crawford;J Am Acad Dermatol,2004

2. Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same;Huq;Fam Cancer,2018

3. Genetic skin diseases predisposing to basal cell carcinoma;Castori;Eur J Dermatol,2012

4. The molecular basis of lipoid proteinosis: mutations in extracellular matrix protein 1;Chan;Exp Dermatol,2007

5. Dermoscopic features of basal cell carcinoma and its subtypes: a systematic review;Reiter;J Am Acad Dermatol,2021

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