Published in:
01-08-2015 | Endocrine Imaging
Pituitary stalk interruption and olfactory bulbs aplasia/hypoplasia in a man with Kallmann syndrome and reversible gonadotrope and somatotrope deficiencies
Authors:
Julie Sarfati, Alexandru Saveanu, Jacques Young
Published in:
Endocrine
|
Issue 3/2015
Login to get access
Excerpt
Kallmann syndrome (KS) is characterized by congenital hypogonadotropic hypogonadism (CHH) and anosmia/hyposmia related to aplasia/hypoplasia of the olfactory bulbs (OB) [
1]. In KS, the gonadotropin deficiency is isolated, the statural growth is preserved and other pituitary functions, particularly growth hormone (GH) secretion are normal, as well as hypothalamo-pituitary morphology [
2]. …