2024
DOI: 10.33925/1683-3031-2024-695
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Orodental manifestations of Noonan syndrome: a clinical case study

T. N. Modina,
E. V. Mamaeva,
M. V. Moseeva
et al.

Abstract: Relevance. Mutations in the PTPN11 gene, a hallmark of Noonan syndrome, disrupt the normal development of connective tissue structure, resulting in a range of manifestations, including orodental abnormalities.Clinical case description. This article presents a medical record of a 14-year-old patient diagnosed with Noonan syndrome who sought medical assistance due to exacerbated chronic generalized periodontitis. The authors implemented a two-stage treatment approach, resulting in satisfactory outcomes. They ide… Show more

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