Most Recent Articles: International Journal of Pediatric Endocrinologyhttps://ijpeonline.biomedcentral.comMost Recent Articles: International Journal of Pediatric EndocrinologyPseudotumor cerebri in patient on leuprolide acetate for central precocious pubertyhttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00092-4Gonadotropin 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 routes of adminis...Case reportThu, 03 Dec 2020 00:00:00 GMThttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00092-4Anjumanara Anver Omar, Godfrey Nyaga and Lucy N Wainaina Mungai2020-12-03T00:00:00ZFanconi Bickel syndrome: clinical phenotypes and genetics in a cohort of Sudanese childrenhttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00091-5Fanconi-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 characterized by a wide spec...ResearchMon, 23 Nov 2020 00:00:00 GMThttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00091-5Salwa A. Musa, Areej A. Ibrahim, Samar S. Hassan, Matthew B Johnson, Asmahan T. Basheer, Ali M. Arabi and Mohamed A. Abdullah2020-11-23T00:00:00ZOutcomes in children treated with growth hormone for Prader-Willi syndrome: data from the ANSWER ProgramĀ® and NordiNetĀ® International Outcome Studyhttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00090-6Growth 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 observational data in pe...ResearchTue, 10 Nov 2020 00:00:00 GMThttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00090-6Moris Angulo, M. Jennifer Abuzzahab, Alberto Pietropoli, Vlady Ostrow, Nicky Kelepouris and Maithe Tauber2020-11-10T00:00:00ZHeight outcomes in children with growth hormone deficiency and idiopathic short stature treated concomitantly with growth hormone and aromatase inhibitor therapy: data from the ANSWER programhttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00089-zTreatment 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 (AIT) blocks estr...ResearchTue, 06 Oct 2020 00:00:00 GMThttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00089-zBradley S. Miller, Judith Ross and Vlady Ostrow2020-10-06T00:00:00ZKlinefelter syndrome and germ cell tumors: review of the literaturehttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00088-0The 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 reports show an inc...ReviewWed, 30 Sep 2020 00:00:00 GMThttps://ijpeonline.biomedcentral.com/articles/10.1186/s13633-020-00088-0Kimberley Bonouvrie, Jutte van der Werff ten Bosch and Machiel van den Akker2020-09-30T00:00:00Z