Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report

Vitamin D-dependent rickets type II is a rare hereditary disorder. It occurs due to mutations in the gene chr. 12q12-q14, which codes for vitamin D receptor. End-organ resistance to 1,25-(OH)(2) vitamin D3 and alopecia in severe cases are the characteristic features. We report a case of a 4-year-old...

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Detalles Bibliográficos
Autores principales: Vupperla, Divya, Lunge, Snehal Balvant, Elaprolu, Praveen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903051/
https://www.ncbi.nlm.nih.gov/pubmed/29692463
http://dx.doi.org/10.4103/ijd.IJD_434_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903051/
https://www.ncbi.nlm.nih.gov/pubmed/29692463
http://dx.doi.org/10.4103/ijd.IJD_434_17

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