Multiple familial pilomatrixomas in the absence of other clinical features: a case of familial benign pilomatrixoma
Author:
Affiliation:
1. Genetic Medicine and Familial Cancer Clinic; Royal Melbourne Hospital; Melbourne Victoria Australia
2. St John of God Pathology; Ballarat Victoria Australia
Publisher
Wiley
Subject
Dermatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/ajd.12233/fullpdf
Reference11 articles.
1. Multiple pilomatricomas: case presentation and review of the literature;Chan;Dermatol. Online J.,2010
2. A common human skin tumour is caused by activating mutations in beta-catenin;Chan;Nat. Genet.,1999
3. Beta-catenin expression in pilomatrixomas: relationship with beta-catenin gene mutations and comparison with beta-catenin expression in normal hair follicles;Moreno-Bueno;Br. J. Dermatol.,2001
4. Acetylation of beta-catenin by CREB-binding protein (CBP);Wolf;J. Biol. Chem.,2002
5. Prevalence of pilomatricoma in Turner syndrome: findings from a multicenter study;Handler;JAMA Dermatol.,2013
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1. Germline Mutation of PLCD1 Contributes to Human Multiple Pilomatricomas through Protein Kinase D/Extracellular Signal–Regulated Kinase1/2 Cascade and TRPV6;Journal of Investigative Dermatology;2021-03
2. Familial papular epidermal nevus with “skyline” basal cell layer and multiple pilomatricomas: A new association?;Pediatric Dermatology;2018-02-28
3. The first case of multiple pilomatricomas caused by somatic mutations of CTNNB1 without any associated disorder;Journal of Dermatological Science;2017-11
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