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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2018
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| Materias: | |
| 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 |