When to suspect a supressor of fused homolog (SUFU)‐associated basal cell nevus syndrome
Author:
Affiliation:
1. Dermatology Department Hospital Clínic Barcelona Spain
2. Universitat de Barcelona Barcelona Spain
3. Plastic Surgery and Maxillofacial Hospital Clínic Barcelona Spain
4. Dermatology Department Clínica Rotger Palma de Mallorca Spain
Publisher
Wiley
Subject
Dermatology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijd.16007
Reference12 articles.
1. Basaloid follicular hamartomas in pediatric Basal Cell Nevus Syndrome: A diagnostic challenge
2. The relevance of a suppressor of fused (SUFU) mutation in the diagnosis and treatment of Gorlin syndrome
3. Multiple Hereditary Infundibulocystic Basal Cell Carcinoma Syndrome Associated With a GermlineSUFUMutation
4. Ameloblastoma: a neglected criterion for nevoid basal cell carcinoma (Gorlin) syndrome
5. Novel SUFU frameshift variant leading to meningioma in three generations in a family with Gorlin syndrome;Askaner G;Case Rep Genet,2019
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1. Clinicopathological and molecular spectrum of patients with germline SUFU mutations: A case series;Journal of Cutaneous Pathology;2024-09-14
2. Mosaic SUFU mutation associated with a mild phenotype of multiple hereditary infundibulocystic basal cell carcinoma syndrome;The Journal of Dermatology;2024-08-19
3. Basaloid Follicular Hamartoma: A Histologic Clue for Diagnosis of Nevoid Basal Cell Carcinoma Syndrome;Dermatologic Surgery;2024-08-13
4. SUFU‐associated Gorlin syndrome: Expanding the spectrum between classic nevoid basal cell carcinoma syndrome and multiple hereditary infundibulocystic basal cell carcinoma;Australasian Journal of Dermatology;2023-02-24
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