An extremely rare association of multiple familial trichoepitheliomas and hereditary multiple osteochondromas-Reference-Cited by-同舟云学术

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An extremely rare association of multiple familial trichoepitheliomas and hereditary multiple osteochondromas

Published:2018-09-23 Issue:12 Volume:57 Page:e157-e159
ISSN:0011-9059
Container-title:International Journal of Dermatology
language:en
Short-container-title:Int J Dermatol

Author:

Monteiro Ana F.¹^ORCID,Saraiva Gil Francisco¹,Rato Margarida¹,Osório Tomás²,Tavares Ermelindo³

Affiliation:

1. Dermatovenereology Department; Hospital de Santarém EPE; Santarém Portugal

2. Department of Orthopedic Surgery; Unidade Local de Saúde do Baixo Alentejo; EPE - Hospital José Joaquim Fernandes; Beja Portugal

3. Dermatovenereology Department; Hospital de Vila Franca de Xira; Vila Franca de Xira Portugal

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijd.14251/fullpdf

Reference10 articles.

1. Brooke-Spiegler syndrome and phenotypic variants: an update;Kazakov;Head Neck Pathol,2016

2. Identification of the cylindromatosis tumor-suppressor gene responsible for multiple familial trichoepithelioma;Zhang;J Invest Dermatol,2004

3. A novel mutation of CYLD in a Chinese family with multiple familial trichoepithelioma;Ying;J Eur Acad Dermatol Venereol,2012

4. Loss of the cylindromatosis tumour suppressor inhibits apoptosis by activating NF-κB;Brummelkamp;Nature,2003

5. CYLD: a tumor suppressor deubiquitinase regulating NF-kappaB activation and diverse biological processes;Sun;Cell Death Differ,2010

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