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Male sickle cell patients, compensated transpubertal hypogonadism and normal final growth.

Paulo Roberto Juliano MartinsFernanda Bernadelli De VitoGláucia Aparecida Domingos ResendeJosé KerbauyGilberto de Araújo PereiraHelio Moraes-SouzaMaria Stella FigueiredoIeda Therezinha Verreschi
Published in: Clinical endocrinology (2019)
These data, in addition to both the clinical and biochemical signs of hypoandrogenism associated with normal to elevated T levels strongly suggest a peripheral origin of hypogonadism, which is probably due to androgen resistance in the patients with SCD.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • newly diagnosed
  • chronic kidney disease
  • replacement therapy
  • peritoneal dialysis
  • electronic health record
  • patient reported outcomes
  • data analysis