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 VerreschiPublished 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.