Cargando…
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),...
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: | |
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 |
Ejemplares similares
-
An Innovative Approach to Evaluate the Morphological Patterns of Soft Palate in Oral Submucous Fibrosis Patients: A Digital Cephalometric Study
por: Raja Lakshmi, Chintamaneni, et al.
Publicado: (2016) -
Hybrid Ameloblastoma of the Maxilla: A Puzzling Pathology
por: Lakshmi, Chintamaneni Raja, et al.
Publicado: (2016) -
Multifocal Epithelial Hyperplasia of Oral Cavity Expressing HPV 16 Gene: A Rare Entity
por: Prabhat, M. P. V., et al.
Publicado: (2013) -
Intraosseous adenoid cystic carcinoma of maxilla: A rare case report
por: Deshpande, Prasannasrinivas Suresh, et al.
Publicado: (2013) -
Association between genetic taste sensitivity, 2D:4D ratio, dental caries prevalence, and salivary flow rate in 6-14-year-old children: a cross-sectional study
por: Lakshmi, Chintamaneni Raja, et al.
Publicado: (2016)