X-Linked Hypophosphatemia at the European Society of Pediatric Endocrinology Meeting 2022

Abstract Rickets, a growth plate disorder, is classified into calcipenic and phosphopenic types based on the etiology. Phosphopenic rickets can be further fibroblast factor 23 (FGF23) mediated non-FGF23 mediated. FGF-23 has phosphaturic effect which results in hypophosphatemia and, therefore, accumulation of hypertrophied chondrocytes, leading to rachitic changes bones. One most common causes inherited hypophosphatemic X-linked (XLH), mainly due mutation PHEX gene that ends extended release FGF-23. During 60th annual meeting European Society for Pediatric Endocrinology, held Rome between September 15 19, 2022, approximately presentations were made either as free communication or poster. In addition, there was dedicated satellite symposium focusing XLH. This article been prepared share knowledge updates discussed during about rickets, we feel this disease still focused MENA region, since are some gaps recognition management FGF23 osteomalacia.