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©The Author(s) 2023.
World J Clin Cases. Aug 16, 2023; 11(23): 5567-5572
Published online Aug 16, 2023. doi: 10.12998/wjcc.v11.i23.5567
Published online Aug 16, 2023. doi: 10.12998/wjcc.v11.i23.5567
Figure 1 Clinical data for the family.
A: Excessive earlobe of the proband; B: Preaxial polydactyly after surgical resection of the proband; C: Toe deformities of the proband; D: Excessive earlobe of the proband’s daughter; E: Preaxial polydactyly after surgical resection of the proband’s daughter.
Figure 2 Identification of the heterozygous variant in the family.
A: Pedigree of the Chinese family. Affected family members are denoted in color. Three members (I-2, II-2 and III-4) underwent genetic study, while others were verified by Sanger sequencing. Arrow indicates the proband; B: Direct Sanger sequencing confirmed the heterozygous variant in SALL1 gene.
- Citation: Wu J, Zhang J, Xiao TL, He T. Townes–Brocks syndrome with adult renal impairment in a Chinese family: A case report. World J Clin Cases 2023; 11(23): 5567-5572
- URL: https://www.wjgnet.com/2307-8960/full/v11/i23/5567.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v11.i23.5567