Hypophosphatemic Rickets in Siblings: A Rare Case Report

Hypophosphatemic rickets (HR) is a type of hereditary rickets characterized by persistent hypophosphatemia and hyperphosphaturia. The most predominant type is inherited in an X-linked fashion and caused by mutation in the gene encoding the phosphate-regulating endopeptidase homolog, X-linked (PHEX),...

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Detalles Bibliográficos
Autores principales: Sarat, Gummadapu, Priyanka, Nuthalapati, Prabhat, Meka Purna Venkata, Raja Lakshmi, Chintamaneni, Bhavana, Sujana Mulk, Ayesha Thabusum, Dharmavaram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906197/
https://www.ncbi.nlm.nih.gov/pubmed/27340574
http://dx.doi.org/10.1155/2016/4803167

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906197/
https://www.ncbi.nlm.nih.gov/pubmed/27340574
http://dx.doi.org/10.1155/2016/4803167

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