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TIO Associated with Hyperparathyroidism: A Rarity, a Rule, or a Novel HPT-PMT Syndrome-A Case Study with Literature Review.

Michael SalimMohannad Samy BehairyElena Barengolts
Published in: Case reports in endocrinology (2021)
The debate whether the patient had pHPT or tertiary HPT prompted literature review showing that aberrant genes including FGFR1, FGF1, fibronectin 1, and Klotho were mechanistically involved in the HPT-PMT association. This case highlights the pitfalls contributing to delayed diagnosis and treatment of TIO and hypothesizes the association between pHPT and PMT.
Keyphrases
  • case report
  • quantum dots
  • visible light
  • genome wide
  • bioinformatics analysis
  • genome wide identification
  • genome wide analysis