An Unusual Combination of Neurological Manifestations and Sudden Vision Loss in a Child with Familial Hyperphosphatemic Tumoral Calcinosis

Hyperphosphatemia in the absence of renal failure is an unusual occurrence, particularly in children, but is a common primary feature of familial hyperphosphatemic tumor calcinosis. We report a child with hyperphosphatemia who presented with multiple episodes of neurologic dysfunction involving lowe...

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Detalles Bibliográficos
Autores principales: Lingappa, Lokesh, Ichikawa, Shoji, Gray, Amie K., Acton, Dena, Evans, Michael J., Madarasu, Rajsekara Chakravarthi, Kekunnaya, Ramesh, Siddaiahagari, Sirisharani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613414/
https://www.ncbi.nlm.nih.gov/pubmed/31359949
http://dx.doi.org/10.4103/aian.AIAN_191_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6613414/
https://www.ncbi.nlm.nih.gov/pubmed/31359949
http://dx.doi.org/10.4103/aian.AIAN_191_18

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