Novel TINF2 gene mutation in dyskeratosis congenita with extremely short telomeres: A case report

doi:10.12998/wjcc.v10.i33.12440

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Nov 26, 2022 (publication date) through Dec 18, 2024

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Nov 26, 2022; 10(33): 12440-12446
Published online Nov 26, 2022. doi: 10.12998/wjcc.v10.i33.12440

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Figure 1 Clinical findings in the patient. A: Dystrophic fingernails; B: Dystrophic toenails; C: White patches on the tongue representing leukoplakia; D: Upper trunk showing reticulate skin pigmentation.

Citation: Picos-Cárdenas VJ, Beltrán-Ontiveros SA, Cruz-Ramos JA, Contreras-Gutiérrez JA, Arámbula-Meraz E, Angulo-Rojo C, Guadrón-Llanos AM, Leal-León EA, Cedano-Prieto DM, Meza-Espinoza JP. Novel TINF2 gene mutation in dyskeratosis congenita with extremely short telomeres: A case report. World J Clin Cases 2022; 10(33): 12440-12446
URL: https://www.wjgnet.com/2307-8960/full/v10/i33/12440.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i33.12440