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Delineation of the phenotypes and genotypes of facial infiltrating lipomatosis associated with PIK3CA mutations.

Hongrui ChenBin SunWei GaoYajing QiuChen HuaXiaoxi Lin
Published in: Orphanet journal of rare diseases (2023)
The abundant clinical presentations and genetic profiles of FIL make it difficult to treat. PIK3CA mutations drive the pathogenesis of FIL, and PIK3CA hotspot mutations may lead to more extensive infiltration of lipomatosis. Understanding the molecular variant profile of FIL will facilitate the application of novel PI3K-targeted inhibitors.
Keyphrases
  • protein kinase
  • genome wide
  • cancer therapy
  • gene expression