Burosumab treatment in a child with cutaneous skeletal hypophosphatemia syndrome: A case report
Author:
Publisher
Elsevier BV
Subject
Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism
Reference24 articles.
1. Diagnosis and management of X-linked hypophosphatemia in children and adolescent in the Gulf cooperationcouncil countries;Al Juraibah;Arch.Osteoporos.,2021
2. Vitamin D-resistant rickets associated with epidermal nevus syndrome: demonstration of a phosphaturic substance in the dermal lesions;Aschinberg;J.Pediatr.,1977
3. FGF23 and its role in X-linked hypophosphatemia-related morbidity;Beck-Nielsen;Orphanet J. Rare Dis.,2019
4. Burosumab therapy in children with X-linkedhypophosphatemia;Carpenter;N.Engl.J.Med.,2018
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1. A child with cutaneous-skeletal hypophosphatemia syndrome caused by a mosaic HRAS mutation – outcome of treatment with anti-FGF23 antibody;2024-07-03
2. Genetic causes of hypophosphatemia;Minerva Medica;2024-06
3. Diagnosis, treatment, and management of rickets: a position statement from the Bone and Mineral Metabolism Group of the Italian Society of Pediatric Endocrinology and Diabetology;Frontiers in Endocrinology;2024-04-19
4. Burosumab for the treatment of cutaneous-skeletal hypophosphatemia syndrome;Bone Reports;2024-03
5. Adult epidermal nevus syndrome with hypophosphatemic osteomalacia treated with burosumab: a case study and literature review;Journal of Cutaneous Immunology and Allergy;2024-02-16
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