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Germinal defects of SDHx genes in patients with isolated pituitary adenoma.

Grégory MougelArnaud LagardeFrédérique AlbarelWassim EssametPerrine LuigiCéline MoulyMagaly VialonThomas CunyFrédéric CastinettiAlexandru SaveanuThierry BrueAnne BarlierPauline Romanet
Published in: European journal of endocrinology (2020)
We discovered SDHx mutations in patients bearing PA who had no familial or personal history of PPGL. However, the question of incidental association remains unresolved and data to determine the benefit of SDHx/MAX screening in these patients are lacking. We recommend that patients with isolated PA should be carefully examined for a family history of PPGLs. A family history of PPGL, as well as the presence of intracytoplasmic vacuoles in PA, requires SDHx/MAX genetic testing of patients.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • chronic kidney disease
  • prognostic factors
  • peritoneal dialysis
  • machine learning
  • genome wide
  • data analysis