hrp0097p2-53 | Bone, Growth Plate and Mineral Metabolism | ESPE2023
Statha Eleni
, Paltoglou George
, Doulgeraki Artemis
, Vakali Eleni
, Vlachopapadopoulou Elpis
, Economou Stavroula
, Sakou Irini-Ikbale
, Soldatou Alexandra
, Karavanaki Kyriaki
, Frysira Elena
Aim: Case report of an 18-month-old child with a background of vitamin D dependent rickets type 1(VDDR1)], due to a mutation of CYP27B1 (c.1319_1325dup and c.335C>T: compound heterozygote).Methods: Presentation of the case and the management of hypocalcemia as well as the complications of follow-up.Results: The patient presented at the A&Es of the 2nd Department of Pediatric...