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Primary Failure Eruption: Genetic Investigation, Diagnosis and Treatment: A Systematic Review.

Inchingolo FrancescoIrene FerraraFabio ViapianoAnna Maria CiociaIrene PalumboMariafrancesca GuglielmoAlessio Danilo InchingoloAndrea PalermoIoana Roxana BordeaAngelo Michele InchingoloDaniela Di VenereGianna Dipalma
Published in: Children (Basel, Switzerland) (2023)
This systematic review provides valuable insights into the diagnosis, treatment, and genetic basis of PFE. Early diagnosis and personalized treatment planning are crucial for successful management. Genetic testing for PTH1R mutations aids in accurate diagnosis and may influence treatment decisions. However, further research is needed to explore the complex genetic basis of PFE fully and improve treatment outcomes for affected individuals.
Keyphrases
  • systematic review
  • genome wide
  • copy number
  • high resolution
  • gene expression
  • combination therapy