Rickets is Not Always Nutritional!
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s12098-023-04808-1.pdf
Reference6 articles.
1. Jacob P, Bhavani GS, Udupa P, et al. Exome sequencing in monogenic forms of rickets. Indian J Pediatr. 2023. https://doi.org/10.1007/s12098-022-04393-9.
2. Beck-Nielsen SS, Brock-Jacobsen B, Gram J, Brixen K, Jensen TK. Incidence and prevalence of nutritional and hereditary rickets in southern Denmark. Eur J Endocrinol. 2009;160:491–7.
3. Cebeci AN, Zou M, BinEssa HA, et al. Mutation of SGK3, a novel regulator of renal phosphate transport, causes autosomal dominant hypophosphatemic rickets. J Clin Endocrinol Metab. 2020;105:1840–50.
4. Reichold M, Klootwijk ED, Reinders J, et al. Glycine amidinotransferase (GATM), renal Fanconi syndrome, and kidney failure. J Am Soc Nephrol. 2018;29:1849–58.
5. Gordon RJ, Li D, Doyle D, Zaritsky J, Levine MA. Digenic heterozygous mutations in SLC34A3 and SLC34A1 cause dominant hypophosphatemic rickets with hypercalciuria. J Clin Endocrinol Metab. 2020;105:2392–400.
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