Characterization of Mineral and Bone Metabolism Biomarkers in a Chinese Consanguineous Twin Family with Primary Hypertrophic Osteoarthropathy.
Na LiYuhang MaYun JiangLi YouYunhong HuangYongde PengXiaoying DingLi ZhaoPublished in: International journal of endocrinology (2020)
The patients with PHO displayed an active state of bone reconstruction. There may be a lack of vitamin D, accompanied by an increase in BGP and β-CTX levels. Heterozygous mutations of SLCO2A1 might lead to mild PHO.