CDKN1C gene mutation causing familial Silver–Russell syndrome: A case report and review of literature

doi:10.12998/wjcc.v11.i19.4655

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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. Jul 6, 2023; 11(19): 4655-4663
Published online Jul 6, 2023. doi: 10.12998/wjcc.v11.i19.4655

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Figure 4 Growth chart of the index patient. Black dots are postnatal height measurements, black arrows indicate initiation of recombinant human growth hormone treatment, and red dots indicate height measurements after growth hormone treatment.

Citation: Li J, Chen LN, He HL. CDKN1C gene mutation causing familial Silver–Russell syndrome: A case report and review of literature. World J Clin Cases 2023; 11(19): 4655-4663
URL: https://www.wjgnet.com/2307-8960/full/v11/i19/4655.htm
DOI: https://dx.doi.org/10.12998/wjcc.v11.i19.4655

Li J, Chen LN, He HL. CDKN1C gene mutation causing familial Silver–Russell syndrome: A case report and review of literature. World J Clin Cases 2023; 11(19): 4655-4663 [PMID: 37469742 DOI: 10.12998/wjcc.v11.i19.4655]

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