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Co-inheritance of Naevoid Basal Cell Carcinoma Syndrome and Neurofibromatosis Type 1 associated with an exceptional spectrum of tumours

Lookup NU author(s): Professor Neil RajanORCiD



This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).


This article is protected by copyright. All rights reserved.The tumours arising in naevoid basal cell carcinoma syndrome (NBCCS) and neurofibromatosis type 1 (NF1) are distinct, and are exemplars of the specific consequences of mutations arising in different tumour suppressor genes. Whilst each syndrome has recognised pathognomonic tumours, an exceptional spectrum of tumours presenting in an individual with either syndrome may represent the interaction of an additional tumour suppressor gene.

Publication metadata

Author(s): Ghadiri SJ, Brennan P, Calonje E, Carmichael AJ, Rajan N

Publication type: Letter

Publication status: Published

Journal: The British Journal of Dermatology

Year: 2020

Volume: 183

Issue: 6

Pages: 1108-1110

Print publication date: 01/12/2020

Online publication date: 20/06/2020

Acceptance date: 10/06/2020

ISSN (print): 0007-0963

ISSN (electronic): 1365-2133

Publisher: NLM (Medline)


DOI: 10.1111/bjd.19324

PubMed id: 32562549