摘要
Objective To analyze the clinical characteristics and molecular mechanisms of 5 cases of hypoparathyroidism caused by GATA3 gene mutation.Methods A total of 5childhood-onset hypoparathyroidism patients with GATA3mutation were identified from 198 hypoparathyroidism(aged≤18 years) from 1975 to 2021 in Peking Union Medical College Hospital. Clinical data and biochemical indices of the 5 patients were collected and analyzed retrospectively.
作者
YANG Jing
杨静(Key Lab Endocrinol,Natl Health Commission,Union Translation Med Center,Dept Endocrinol,PCMC&CAMS,Beijing 100730)
