Congenital Hypogonadotrophic Hypogonadism: Minipuberty and the Case for Neonatal Diagnosis

Congenital Hypogonadotrophic Hypogonadism: Minipuberty and the Case for Neonatal Diagnosis

Congenital hypogonadotrophic hypogonadism (CHH) is a rare but important etiology of pubertal failure and infertility, resulting from impaired gonadotrophin-releasing hormone secretion or action. Despite the availability of effective hormonal therapies, the majority of men with CHH experience unsatis...

Full description

Bibliographic Details
Main Authors: Du Soon Swee, Richard Quinton
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-02-01
Series:Frontiers in Endocrinology
Subjects:
congenital hypogonadotropic hypogonadism
kallmann syndrome
puberty delay
minipuberty of infancy
infertility–male
cryptorchidism
Online Access:https://www.frontiersin.org/article/10.3389/fendo.2019.00097/full

Internet

https://www.frontiersin.org/article/10.3389/fendo.2019.00097/full

Similar Items