Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report

doi:10.12998/wjcc.v11.i9.2036

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Mar 26, 2023 (publication date) through Nov 4, 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. Mar 26, 2023; 11(9): 2036-2042
Published online Mar 26, 2023. doi: 10.12998/wjcc.v11.i9.2036

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Figure 2 Distinctive facial features. A: Round face, stubby nose, forward-leaned nostrils and thick lips; B: Long eyelashes.

Citation: Shen R, Feng JH, Yang SP. Acromicric dysplasia caused by a mutation of fibrillin 1 in a family: A case report. World J Clin Cases 2023; 11(9): 2036-2042
URL: https://www.wjgnet.com/2307-8960/full/v11/i9/2036.htm
DOI: https://dx.doi.org/10.12998/wjcc.v11.i9.2036