Gonadotropin releasing hormone agonists (GnRHa) are well established as a standard of care for the treatment of central precocious puberty (CPP) worldwide. While numerous delivery systems and rou...
https://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00092-4
Fanconi-Bickel syndrome (FBS) is a rare condition of carbohydrate metabolism, caused by a recessive defect in the facilitative glucose transporter GLUT2 encoded by the SLC2A2 gene and characteriz...
https://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00091-5
Growth hormone (GH) deficiency is common in patients with Prader-Willi syndrome (PWS) and leads to short adult stature. The current study assessed clinical outcomes based on real-world observatio...
https://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00090-6
Treatment of children with growth hormone deficiency (GHD) or idiopathic short stature (ISS) using GH is only effective for bone growth prior to epiphyseal fusion. Aromatase inhibitor therapy (AI...
https://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00089-z
The most common presentation of Klinefelter syndrome (KS) is infertility and features of hypogonadism. Currently no consensus exists on the risk of malignancy in this syndrome. Several case repor...
https://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00088-0