Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Editorial
. 2023 Dec;90(12):1169-1170.
doi: 10.1007/s12098-023-04808-1. Epub 2023 Sep 4.

Rickets is Not Always Nutritional!

Selvamanojkumar S  1 , Neerja Gupta  2
Affiliations
Editorial

Rickets is Not Always Nutritional!

Selvamanojkumar S et al. Indian J Pediatr. 2023 Dec.
No abstract available

PubMed Disclaimer

References

    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 . - DOI - PubMed
    1. 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. - DOI - PubMed
    1. 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. - DOI
    1. 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. - DOI - PubMed - PMC
    1. 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. - DOI - PubMed - PMC

Publication types