Searchable abstracts of presentations at key conferences in endocrinology

ea0073aep591 | Reproductive and Developmental Endocrinology | ECE2021

Hypogonadotropic hypogonadism revealing a classic form of 21 hydroxylase deficiency in a 39 year old man

Alassane Ilboudo , Carine Courtillot , Yempabou Sagnan , Sophie Dubreuil , Touraine Philippe

Classical forms of 21 hydroxylase defisciency are generally observed during bith life and present as loss of salt or rapid puberty in young boy. We report a rare case of classical 21 hydroxylase defisciency presented as low gonadotrophines contrasted with normal level of testosterone. This was related to a 39 years old patient consulted for male infertility. Clinical exam was normal, including a normal level of blood tension. Liquid chromatography–tandem mass spectrometry...

ea0073aep859 | Late Breaking | ECE2021

Infertility revealing a classical form of congenital adrenal hyperplasia in a 39 years old man

Alassane Ilboudo , Yempabou Sagnan , Mathilde Guigui , Sophie Dubreuil , Antonin Lamaziere , Bachelot Anne , Touraine Philippe , Carine Courtillot

Classical forms of congenital adrenal hyperplasia (CAH) are generally diagnosed in neonates (salt wasting form) or in early childhood (pure virilizing form). Here, we report the case of a 39 years old man from Sri Lanka in whom a classical CAH has been diagnosed during the exploration of infertility with azoospermia, along with extremely low gonadotropins contrasting with a normal level of testosterone. Hormonal tests revealed high serum 17-hydroxyprogesterone levels (255 ng/m...