Searchable abstracts of presentations at key conferences in endocrinology

ea0081p297 | Calcium and Bone | ECE2022

Phenotype characterization of a PHEX non canonical splice-site mutation in a family affected by X linked hypophosphatemic rickets and efficacy of one-year Burosumab treatment in adult patients

Di Fraia Rosa , Digitale Selvaggio Lucia , Allosso Francesca , Pasquali Daniela

X-linked hypophosphatemic rickets (XLH) is associated with mutations in PHEX, upregulation of FGF23, leading to hypophosphatemia, abnormal bone development and short stature. H-MAB to FGF23, Burosumab, is the new therapy for XLH. Among PHEX mutations, c.1586+6T >C, partially destroying the splice-site, is presumably associated to a mild phenotype not described so far. We describe two siblings bearing the PHEX c.1586+6T >C variant. Cas...

ea0081p702 | Reproductive and Developmental Endocrinology | ECE2022

Non-alcoholic fatty liver disease prevalence in Klinefelter syndrome

Digitale Selvaggio Lucia , Di Fraia Rosa , Allosso Francesca , Marrone Aldo , Pasquali Daniela

Non-alcoholic fatty liver disease (NAFLD) is becoming more common over the world. Its predisposition for evolving to cirrhosis and hepatocellular cancer, as well as its link to extrahepatic symptoms, puts patients and clinicians under a double burden. Several studies have found a link between NAFLD and many endocrinopathies, demonstrating a substantial bi-directional link between NAFLD and hypogonadism, in both men and women. In man with T2DM, NAFLD is linked to reduced total ...