Alteration of Bone Microarchitecture in Hereditary Distal RTA Patients With <i>SLC4A1</i> Gene Mutation: Assessed by HR-pQCT
Skeletal lesions were common clinical manifestations in SLC4A1-dRTA patients. Compared with XLH, another common type of rickets, SLC4A1-dRTA patients had more severe trabecular bone microstructure damage, further supporting the necessity of early diagnosis and timely treatment of the disease.
Authors
- Xiaoping Xing (ORCID: https://orcid.org/0000-0002-2759-5177)
- Weibo Xia (ORCID: https://orcid.org/0000-0001-7768-5536)
- Yan Jiang (ORCID: https://orcid.org/0000-0003-4434-3462)
- Mei Li (ORCID: https://orcid.org/0000-0001-8634-2252)
- Juan Du (ORCID: https://orcid.org/0000-0002-0271-1709)
- Ou Wang (ORCID: https://orcid.org/0000-0002-0395-8789)
- Shujie Zhang (ORCID: https://orcid.org/0000-0003-4880-9856)
- Rong Chen (ORCID: https://orcid.org/0000-0003-3759-4984)
- Lijia Cui (ORCID: https://orcid.org/0000-0002-9929-340X)
Institutions
- Handan College (CN)
- Shanghai Jiao Tong University (CN)
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Peking Union Medical College Hospital (CN)
- Tongren Hospital (CN)
Publication Details
- Journal
- The Journal of Clinical Endocrinology & Metabolism
- Published
- 2024-08-16
- DOI
- https://doi.org/10.1210/clinem/dgae533
- Citations
- 2
- Primary Topic
- Ion Transport and Channel Regulation
- Type
- article
- Field-Weighted Citation Impact
- 0.47
Funders
- National Natural Science Foundation of China
- Chinese Academy of Medical Sciences
- National Key Research and Development Program of China Stem Cell and Translational Research