Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma.

doi:10.1155/2022/7840710

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Article

Association between Mutation in SMARCAD1 and Basan Syndrome with Cutaneous Squamous Cell Carcinoma.

Disease markers - 1 Jan 2022

Xiong Ying, Chen Ting, Yu Jia, Zhou He, Lu Baozhen, Chen Lijie, Sun Liwei, Wang Can, Li Sujun, Wu Bo

Abstract excerpt

Background: Basan syndrome is a rare autosomal-dominant ectodermal dysplasia with certain clinic-pathological features caused by mutations in the SMARCAD1 gene. Currently, no skin malignancy related to Basan syndrome has been reported. This study was aimed at identifying related gene mutations in a new Chinese pedigree with Basan syndrome and discovering the possible association between Basan syndrome and...

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PMID: 35592705
DOI: 10.1155/2022/7840710
PMCID: PMC9113868

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